[Title 16 CFR A]
[Code of Federal Regulations (annual edition) - January 1, 2002 Edition]
[Title 16 - COMMERCIAL PRACTICES]
[Chapter II - CONSUMER PRODUCT SAFETY COMMISSION]
[Subchapter A - GENERAL]
[From the U.S. Government Printing Office]


16COMMERCIAL PRACTICES22002-01-012002-01-01falseGENERALASUBCHAPTER ACOMMERCIAL PRACTICESCONSUMER PRODUCT SAFETY COMMISSION
                          SUBCHAPTER A--GENERAL


PART 1000--COMMISSION ORGANIZATION AND FUNCTIONS--Table of Contents




Sec.
1000.1 The Commission.
1000.2 Laws administered.
1000.3 Hotline.
1000.4 Commission address.
1000.5 Petitions.
1000.6 Commission decisions and records.
1000.7 Advisory opinions and interpretations of regulations.
1000.8 Meetings and hearings; public notice.
1000.9 Quorum.
1000.10 The Chairman and Vice Chairman.
1000.11 Delegation of functions.
1000.12 Organizational structure.
1000.13 Directives system.
1000.14 Office of the General Counsel.
1000.15 Office of Congressional Relations.
1000.16 Office of the Secretary.
1000.17 Office of the Inspector General.
1000.18 Office of Equal Employment Opportunity and Minority Enterprise.
1000.19 Office of Executive Director.
1000.20 Office of the Budget.
1000.21 Office of Hazard Identification and Reduction.
1000.22 Office of Planning and Evaluation.
1000.23 Office of Information and Public Affairs.
1000.24 Office of Compliance.
1000.25 Office of Human Resources Management.
1000.26 Office of Information Services.
1000.27 Directorate for Epidemiology.
1000.28 Directorate for Health Sciences.
1000.29 Directorate for Economic Analysis.
1000.30 Directorate for Engineering Sciences.
1000.31 Directorate for Laboratory Sciences.
1000.32 Directorate for Administration.
1000.33 Directorate for Field Operations.

    Authority: 5 U.S.C. 552(a).

    Source: 56 FR 30496, July 3, 1991, unless otherwise noted.



Sec. 1000.1  The Commission.

    (a) The Consumer Product Safety Commission is an independent 
regulatory agency which was formed on May 14, 1973, under the provisions 
of the Consumer Product Safety Act (Pub. L. 92-573, 86 Stat. 1207, as 
amended (15 U.S.C. 2051, et seq.)). The purposes of the Commission under 
the CPSA are:
    (1) To protect the public against unreasonable risks of injury 
associated with consumer products;
    (2) To assist consumers in evaluating the comparative safety of 
consumer products;
    (3) To develop uniform safety standards for consumer products and to 
minimize conflicting State and local regulations; and
    (4) To promote research and investigation into the causes and 
prevention of product-related deaths, illnesses, and injuries.
    (b) The Commission is composed of five members appointed by the 
President, by and with the advice and consent of the Senate, for terms 
of seven years.



Sec. 1000.2  Laws administered.

    The Commission administers five acts:
    (a) The Consumer Product Safety Act (Pub. L. 92-573, 86 Stat. 1207, 
as amended (15 U.S.C. 2051, et seq.)).
    (b) The Flammable Fabrics Act (Pub. L. 90-189, 67 Stat. 111, as 
amended (15 U.S.C. 1191, et seq.)).
    (c) The Federal Hazardous Substances Act (Pub. L. 86-613, 74 Stat. 
380, as amended (15 U.S.C. 1261, et seq.)).
    (d) The Poison Prevention Packaging Act of 1970 (Pub. L. 91-601, 84 
Stat. 1670, as amended (15 U.S.C. 1471, et seq.)).
    (e) The Refrigerator Safety Act of 1956 (Pub. L. 84-930, 70 Stat. 
953, (15 U.S.C. 1211, et seq.)).



Sec. 1000.3  Hotline.

    (a) The Commission operates a toll-free telephone Hotline by which 
the public can communicate with the Commission. The number for use in 
all 50 states is 1-800-638-CPSC (1-800-638-2772).
    (b) The Commission also operates a toll-free Hotline by which 
hearing or speech-impaired persons can communicate by teletypewriter 
with the Commission. The teletypewriter number for use in all states is 
1-800-638-8270.
    (c) The Commission also makes information available to the public 
product recall information, its public calendar, and other information 
through its

[[Page 8]]

Internet gopher service at Internet address cpsc.gov. The public may 
also report product hazards or other information to the Commission at 
its electronic mail address: [email protected].
    (d) The Commission also provides a fax-on-demand service from which 
the public can request Commission documents by calling 1-301-504-0051 
from the handset of a facsimile machine.

[56 FR 30496, July 3, 1991, as amended at 59 FR 66673, Dec. 28, 1994]



Sec. 1000.4  Commission address.

    (a) The principal Offices of the Commission are at 4330 East West 
Highway, Bethesda, Maryland. All U.S. Postal Service mail communications 
with the Commission should be addressed to the Consumer Product Safety 
Commission, Washington, DC 20207-0001, unless otherwise specifically 
directed. Materials sent by private express services or by messenger 
should be addressed to the Consumer Product Safety Commission, 4330 East 
West Highway, Bethesda, Maryland 20814-4408.
    (b) The Commission has 3 Regional Centers which are located at the 
following addresses and which serve the states and territories 
indicated:
    (1) Central Regional Center, 230 South Dearborn St., room 2944, 
Chicago, Illinois 60604-1601; Alabama, Georgia, Illinois, Indiana, Iowa, 
Kansas, Kentucky, Michigan, Minnesota, Mississippi, Missouri, Nebraska, 
North Dakota, Ohio, South Dakota, Tennessee, and Wisconsin.
    (2) Eastern Regional Center, 6 World Trade Center, Vesey Street, 
room 350, New York, New York 10048-0950; Connecticut, Delaware, District 
of Columbia, Florida, Maine, Maryland, Massachusetts, New Hampshire, New 
Jersey, New York, North Carolina, Pennsylvania, Puerto Rico, Rhode 
Island, South Carolina, Vermont, Virginia, West Virginia, and Virgin 
Islands.
    (3) Western Regional Center, 600 Harrison St., room 245, San 
Francisco, California 94107-1370; Alaska, American Samoa, Arizona, 
Arkansas, California, Colorado, Guam, Hawaii, Idaho, Louisiana, Montana, 
Nevada, New Mexicao, Oklahoma, Oregon, Texas, Utah, Washington, and 
Wyoming.

[56 FR 30496, July 3, 1991; 56 FR 67174, Dec. 30, 1991, as amended at 58 
FR 64120, Dec. 6, 1993; 59 FR 66673, Dec. 28, 1994]



Sec. 1000.5  Petitions.

    Any interested person may petition the Commission to issue, amend, 
or revoke a rule or regulation by submitting a written request to the 
Secretary, Consumer Product Safety Commission, Washington, DC 20207.



Sec. 1000.6  Commission decisions and records.

    (a) Each decision of the Commission, acting in an official capacity 
as a collegial body, is recorded in Minutes of Commission meetings or as 
a separate Record of Commission Action. Copies of Minutes or of a Record 
of Commission Action may be obtained upon written request from the 
Secretary, Consumer Product Safety Commission, Washington, DC 20207, or 
may be examined in the public reading room at Commission headquarters. 
Requests should identify the subject matter of the Commission action and 
the approximate date of the Commission action, if known.
    (b) Other records in the custody of the Commission may be requested 
in writing from the Office of the Secretary pursuant to the Commission's 
Procedures for Disclosure or Production of Information under the Freedom 
of Information Act (16 CFR part 1015).



Sec. 1000.7  Advisory opinions and interpretations of regulations.

    (a) Advisory opinions. Upon written request, the General Counsel 
provides written advisory opinions interpreting the acts the Commission 
administers. Advisory opinions represent the legal opinions of the 
General Counsel and may be changed or superseded by the Commission. 
Requests for issuance of advisory opinions should be sent to the General 
Counsel, Consumer Product Safety Commission, Washington, DC 20207. 
Requests for copies of particular previously issued advisory opinions or 
a copy of an index of such opinions should be submitted to the Office of 
the Secretary, Consumer Product Safety Commission, Washington, DC 20207.

[[Page 9]]

    (b) Interpretations of regulations. Upon written request, the 
Assistant Executive Director for Compliance will issue written 
interpretations of Commission regulations pertaining to the safety 
standards and the enforcement of those standards. Interpretations of 
regulations represent the interpretations of the staff and may be 
changed or superseded by the Commission. Requests for such 
interpretations should be sent to the Assistant Executive Director for 
Compliance, Consumer Product Safety Commission, Washington, DC 20207. 
Requests for interpretations of administrative regulations (e.g., 
Freedom of Information Act regulations) should be sent to the Secretary, 
Consumer Product Safety Commission, Washington, DC 20207.

[56 FR 30496, July 3, 1991, as amended at 60 FR 26825, May 19, 1995]



Sec. 1000.8  Meetings and hearings; public notice.

    (a) The Commission may meet and exercise all its powers in any 
place.
    (b) Meetings of the Commission are held as ordered by the Commission 
and, unless otherwise ordered, are held at the principal office of the 
Commission at 4330 East West Highway, Bethesda, Maryland. Meetings of 
the Commission for the purpose of jointly conducting the formal business 
of the agency, including the rendering of official decisions, are 
generally announced in advanced and open to the public, as provided by 
the Government in the Sunshine Act (5 U.S.C. 552b) and the Commission's 
Meetings Policy (16 CFR part 1012).
    (c) The Commission may conduct any hearing or other inquiry 
necessary or appropriate to its functions anywhere in the United States. 
It will publish a notice of any proposed hearing in the Federal Register 
and will afford a reasonable opportunity for interested persons to 
present relevant testimony and data.
    (d) Notices of Commission meetings, Commission hearings, and other 
Commission activities are published in a Public Calendar, as provided in 
the Commission's Meetings Policy (16 CFR part 1012).

[56 FR 30496, July 3, 1991, as amended at 62 FR 46667, Sept. 4, 1997]



Sec. 1000.9  Quorum.

    Three members of the Commission constitute a quorum for the 
transaction of business. If there are only three members serving on the 
Commission because of vacancies, two members constitute a quorum. If 
there are only two members serving on the Commission because of 
vacancies, two members constitute a quorum, but only for six months from 
the time the number of members was reduced to two.



Sec. 1000.10  The Chairman and Vice Chairman.

    (a) The Chairman is the principal executive officer of the 
Commission and, subject to the general policies of the Commission and to 
such regulatory decisions, findings, and determinations as the 
Commission is by law authorized to make, he or she exercises all of the 
executive and administrative functions of the Commission.
    (b) The Commission annually elects a Vice Chairman to act in the 
absence or disability of the Chairman or in case of a vacancy in the 
Office of the Chairman.



Sec. 1000.11  Delegation of functions.

    Section 27(b)(9) of the Consumer Product Safety Act (15 U.S.C. 
2076(b)(9)) authorizes the Commission to delegate any of its functions 
and powers, other than the power to issue subpoenas, to any officer or 
employee of the Commission. Delegations are published in the 
Commission's Directives System.



Sec. 1000.12  Organizational structure.

    The Consumer Product Safety Commission is composed of the principal 
units listed in this section.
    (a) The following units report directly to the Chairman of the 
Commission:
    (1) Office of the General Counsel;
    (2) Office of Congressional Relations;
    (3) Office of the Secretary;
    (4) Office of the Inspector General;
    (5) Office of Equal Employment Opportunity and Minority Enterprise;
    (6) Office of the Executive Director.
    (b) The following units report directly to the Executive Director of 
the Commission:

[[Page 10]]

    (1) Office of the Budget;
    (2) Office of Hazard Identification and Reduction;
    (3) Office of Information and Public Affairs;
    (4) Office of Compliance;
    (5) Office of Planning and Evaluation;
    (6) Office of Human Resources Management;
    (7) Office of Information Services;
    (8) Directorate for Administration;
    (9) Directorate for Field Operations.
    (c) The following units report directly to the Assistant Executive 
Director for Hazard Identification and Reduction:
    (1) Directorate for Economic Analysis;
    (2) Directorate for Epidemiology;
    (3) Directorate for Health Sciences;
    (4) Directorate for Engineering Sciences;
    (5) Directorate for Laboratory Sciences.

[61 FR 1707, Jan. 23, 1996, as amended at 64 FR 66579, Nov. 29, 1999]



Sec. 1000.13  Directives system.

    The Commission maintains a Directives System which contains 
delegations of authority and descriptions of Commission programs, 
policies, and procedures. A complete set of directives is available for 
inspection in the public reading room at Commission headquarters.



Sec. 1000.14  Office of the General Counsel.

    The Office of the General Counsel provides advice and counsel to the 
Commissioners and organizational components of the Commission on matters 
of law arising from operations of the Commission. It prepares the 
Commission's legislative program and comments on relevant legislative 
proposals originating elsewhere. The Office, in conjunction with the 
Department of Justice, is responsible for the conduct of all Federal 
court litigation to which the Commission is a party. The Office also 
advises the Commission on administrative litigation matters. The Office 
provides final legal review of and makes recommendations to the 
Commission on proposed product safety standards, rules, regulations, 
petition actions, and substantial hazard actions. It also provides legal 
review of certain procurement, personnel, and administrative actions and 
drafts documents for publication in the Federal Register.



Sec. 1000.15  Office of Congressional Relations.

    The Office of Congressional Relations is the principal contact with 
the committees and members of Congress. It performs liaison duties for 
the Commission, provides information and assistance to Congress on 
matters of Commission policy, and coordinates testimony and appearances 
by Commissioners and agency personnel before Congress.



Sec. 1000.16  Office of the Secretary.

    The Office of the Secretary prepares the Commission's agenda, 
schedules and coordinates Commission business at official meetings, and 
records, issues, and stores the official records of Commission actions. 
The Office prepares and publishes the Public Calendar under the 
Commission's Meetings Policy. The Office exercises joint responsibility 
with the Office of the General Counsel for the interpretation and 
application of the Privacy Act, Freedom of Information Act, and the 
Government in the Sunshine Act, and prepares reports required by these 
acts. It issues Commission decisions, orders, rules, and other official 
documents, including Federal Register notices, for and on behalf of the 
Commission and controls the use of the Commission seal. The Secretary of 
the Commission also serves as the agency's Advisory Committee Management 
Officer, and is responsible for managing the establishment, procedures, 
and accomplishments of all advisory committees utilized by the 
Commission. The Office supervises and administers the dockets of 
adjudicative proceedings before the Commission. The Office maintains the 
records of continuing guaranties of compliance with applicable standards 
of flammability issued under the Flammable Fabrics Act (FFA) which are 
filed with the Commission in accordance with provisions of section 8(a) 
of the FFA (15 U.S.C. 1197(a)). Upon request, the Office of the 
Secretary provides appropriate forms to persons and

[[Page 11]]

firms desiring to execute continuing guaranties under the FFA. The 
Office also supervises and administers the public reading room.



Sec. 1000.17  Office of the Inspector General.

    The Office of the Inspector General is an independent office 
established under the provisions of the Inspector General Act of 1978, 5 
U.S.C. appendix, as amended by the Inspector General Act Amendments of 
1988. This Office independently initiates, conducts, supervises, and 
coordinates audits, operations reviews, and investigations of Commission 
programs, activities, and operations. Reporting only to the Chairman, 
and under his or her general supervision, the Office also makes 
recommendations to promote economy, efficiency, and effectiveness within 
the Commission's programs and operations. The Office receives and 
investigates complaints or information concerning possible violations of 
law, rules, or regulations, mismanagement, abuse of authority, and waste 
of funds. It reviews existing and proposed legislation concerning the 
economy, efficiency, and effectiveness of such legislation on Commission 
operations.



Sec. 1000.18  Office of Equal Employment Opportunity and Minority Enterprise.

    The Office of Equal Employment Opportunity and Minority Enterprise 
assures compliance with all laws and regulations relating to equal 
employment opportunity in accordance with the Equal Employment Act of 
1972, 29 CFR part 1613, and section 8(a) of the Small Business Act. The 
Office reports directly to the Chairman and provides advice to the 
Chairman and Commission staff on EEO matters and the agency Procurement 
Preference Program. The Office manages the discrimination complaint 
process, the Upward Mobility Program, the stay-in-school program, and 
other special emphasis activities having to do with affirmative action 
employment practices. The Office makes recommendations to the Chairman 
on ways to promote equal opportunity in order to enhance the 
Commission's EEO posture.



Sec. 1000.19  Office of Executive Director.

    The Executive Director with the assistance of the Deputy Executive 
Director, under the broad direction of the Chairman and in accordance 
with Commission policy, acts as the chief operating manager of the 
agency, supporting the development of the agency's budget and operating 
plan before and after Commission approval, and managing the execution of 
those plans. The Executive Director has direct line authority over the 
following directorates and offices: the Directorate for Administration, 
the Directorate for Field Operations, the Office of the Budget, the 
Office of Hazard Identification and Reduction, the Office of Information 
and Public Affairs, the Office of Compliance, the Office of Planning and 
Evaluation, the Office of Human Resources Management, and the Office of 
Information Services.

[59 FR 66673, Dec. 28, 1994, as amended at 60 FR 26825, May 19, 1995]



Sec. 1000.20  Office of the Budget.

    The Office of the Budget is responsible for overseeing the 
development of the Commission's budget. The Office, in consultation with 
other offices and directorates, prepares, for the Commission's approval, 
the annual budget requests to Congress and the Office of Management and 
Budget and the operating plans for each fiscal year. It manages the 
execution of the Commission's budget. The Office recommends to the 
Office of the Executive Director actions to enhance effectiveness of the 
Commission's programs and activities.



Sec. 1000.21  Office of Hazard Identification and Reduction.

    The Office of Hazard Identification and Reduction, under the 
direction of the Assistant Executive Director for Hazard Identification 
and Reduction, is responsible for managing the Commission's Hazard 
Identification and Analysis Program and its Hazard Assessment and 
Reduction Program. The Office reports to the Executive Director, and has 
line authority over the Directorates for Epidemiology and Health 
Sciences, Economic Analysis, Engineering Sciences, and Laboratory

[[Page 12]]

Sciences. The Office develops strategies for and implements the agency's 
operating plans for these two hazard programs. This includes the 
collection and analysis of data to identify hazards and hazard patterns, 
the implementation of the Commission's safety standards development 
projects, the coordination of voluntary standards activities and 
international liaison activities related to consumer product safety, and 
providing overall direction and evaluation of projects involving hazard 
analysis, data collection, emerging hazards, mandatory and voluntary 
standards, petitions, and labeling rules. The Office assures that 
relevant technical, environmental, economic, and social impacts of 
projects are comprehensively and objectively presented to the Commission 
for decision.

[56 FR 30496, July 3, 1991, as amended at 61 FR 1708, Jan. 23, 1996]



Sec. 1000.22  Office of Planning and Evaluation.

    The Office of Planning and Evaluation reports to the Executive 
Director and is responsible for the Commission's planning and evaluation 
activities. It develops integrated short and long range plans for 
achieving the Commission's goals and objectives. The office is 
responsible for the development and analysis of both major policy and 
operational issues. Evaluation studies are conducted to determine how 
well the Commission fulfills its mission. These studies include impact 
and process evaluations of Commission programs, projects, functions, and 
activities. Recommendations are made to the Executive Director for 
changes to improve their efficiency and effectiveness. Management 
analyses and special studies are also conducted. These cover, but are 
not limited to, internal controls, organizational performance, 
structure, and productivity measurement. Recommendations are made to the 
Executive Director for improving management efficiency and 
effectiveness. The Office also coordinates, develops, and issues 
agencywide directives and manages the Commission's information 
collection budget and obtains Office of Management and Budget clearance 
for information collections.



Sec. 1000.23  Office of Information and Public Affairs.

    The Office of Information and Public Affairs, which is managed by 
the Director of the Office, is responsible for the development, 
implementation, and evaluation of a comprehensive national information 
and public affairs program designed to promote product safety. This 
includes responsibility for developing and maintaining relations with a 
wide range of national groups such as consumer organizations; business 
groups; trade associations; state and local government entities; labor 
organizations; medical, legal, scientific and other professional 
associations; and other Federal health, safety and consumer agencies. 
The Office also is responsible for implementing the Commission's media 
relations program nationwide. The Office serves as the Commission's 
spokesperson to the national print and broadcast media, develops and 
disseminates the Commission's news releases, and organizes Commission 
news conferences.

[59 FR 66673, Dec. 28, 1994]



Sec. 1000.24  Office of Compliance.

    The Office of Compliance, which is managed by the Assistant 
Executive Director for Compliance, conducts or supervises the conduct of 
compliance and administrative enforcement activity under all 
administered acts, provides advice and guidance to regulated industries 
on complying with all administered acts and reviews proposed standards 
and rules with respect to their enforceability. The Office's 
responsibility also includes identifying and acting on safety hazards in 
consumer products already in distribution, promoting industry compliance 
with existing safety rules, and conducting litigation before an 
administrative law judge relative to administrative complaints. It 
directs the enforcement efforts of the field offices and provides 
program guidance, advice, and case guidance to field offices and 
participates in the development of standards before their promulgation 
to assure enforceability of the final product. It enforces the Consumer 
Product Safety Act requirement that firms identify and report product 
defects which could

[[Page 13]]

present possible substantial hazards, violations of consumer product 
safety rules, violations of standards relied upon by the Commission, or 
unreasonable risk of serious injury or death, and the requirement that 
firms report certain lawsuit information. It reviews consumer 
complaints, in-depth investigations, and other data to identify those 
consumer products containing such hazards or which do not comply with 
existing safety requirements. The Office negotiates and subsequently 
monitors corrective action plans designed to give public notice of 
hazards and recall defective or non-complying products subject to the 
Commission's jurisdiction, gives public warning to consumers where 
appropriate, and provides guidelines and directs the field in 
negotiating and monitoring corrective action plans designed to recall 
products which fail to comply with specific regulations. It gathers 
information on generic product hazards which may lead to subsequent 
initiation of safety standard setting procedures. The Office develops 
surveillance strategies and programs designed to assure compliance with 
Commission standards and regulations. It originates instructions to 
field offices and provides subsequent interpretations or guidance for 
field surveillance and enforcement activities.

[56 FR 30496, July 3, 1991, as amended at 60 FR 26825, May 19, 1995]



Sec. 1000.25  Office of Human Resources Management.

    The Office of Human Resources Management, which is managed by the 
Director of the Office, provides human resources management support to 
the Commission in the areas of recruitment and placement, position 
classification, training and executive development, employee and labor 
relations, employee benefits and retirement assistance, employee 
assistance programs, drug testing, leave administration, disciplinary 
and adverse actions, grievances and appeals, and performance management.

[59 FR 66673, Dec. 28, 1994]



Sec. 1000.26  Office of Information Services.

    The Office of Information Services, which is managed by the 
Assistant Executive Director for Information Services, is responsible 
for general policy, controlling and conducting managerial activities and 
operations relating to the collection, use, and dissemination of 
information by the agency. The Office manages the Commission's 
information system that supports all its program activities. The Office 
provides automated data processing and operational support for data 
collection, information retrieval, report generation, electronic mail, 
and statistical and mathematical operations of the agency. The Office 
maintains the agency's local and wide area networks and develops and 
supports other network applications. The Office develops plans for 
improving agency operations through the use of information technology. 
The Office's functional responsibilities include planning, organizing, 
and directing information resources management (including records 
management and related requirements), and the managing of the agency's 
management directives system. The Office administers the Commission's 
telecommunications services including the agency's toll-free Hotline by 
which the public reports hazardous consumer products and receives 
information about product recalls and product hazards. It also oversees 
operation of the Commission's Internet and fax-on-demand services.

[61 FR 1707, Jan. 23, 1996, as amended at 66 FR 38369, July 24, 2001]



Sec. 1000.27  Directorate for Epidemiology.

    The Directorate for Epidemiology, managed by the Associate Executive 
Director for Epidemiology, is responsible for the collection and 
analysis of data on injuries and deaths associated with consumer 
products. The Directorate has two divisions: the Data Systems Division 
and the Hazard Analysis Division. The Data Systems Division operates the 
national data collection systems which provide the data that serve as 
the basis for the Commission's estimates of the numbers of deaths and 
injuries associated with consumer

[[Page 14]]

products. These data systems include the National Electronic Injury 
Surveillance System, a nationally representative sample of hospital 
emergency departments; a death certificate file, which contains data 
obtained from death certificates on deaths associated with consumer 
products; and the Injury and Potential Injury Incident file, which 
contains information on incidents associated with consumer products, 
based on news clips, medical examiner reports, hotline reports, internet 
complaints, referrals, etc. The Hazard Analysis Division conducts 
statistical analysis of these data and conducts epidemiologic studies to 
estimate the numbers of injuries and deaths associated with various 
consumer products and to examine factors associated with these injuries 
and deaths. In addition, staff in the Hazard Analysis Division design 
special studies, design and analyze data from experiments for testing of 
consumer products, and provide statistical expertise and advice to 
Commission staff in support of regulation development. It administers 
the National Injury Information Clearinghouse.

[64 FR 66579, Nov. 29, 1999, as amended at 66 FR 38369, July 24, 2001]



Sec. 1000.28  Directorate for Health Sciences.

    The Directorate for Health Sciences is managed by the Associate 
Executive Director for Health Sciences and is responsible for reviewing 
and evaluating the human health effects and hazards related to consumer 
products and assessing exposure, uptake and metabolism, including 
information on population segments at risk. Directorate staff conducts 
health studies and research in the field of consumer product-related 
injuries. The Directorate performs risk assessments for chemical, 
physiological and physical hazards based on methods such as medical 
injury modeling, and on injury and incident data for mechanical, 
thermal, chemical and electrical hazards in consumer products. It 
provides the Commission's primary source of scientific expertise for 
implementation of the Poison Prevention Packaging Act and the Federal 
Hazardous Substances Act. The Directorate assists in the development and 
evaluation of product safety standards and test methods based on 
scientific and public health principles. It provides support to the 
Commission's regulatory development and enforcement activities. It 
manages hazard identification and analysis, and hazard assessment and 
reduction projects as assigned. The Directorate provides liaison with 
the National Toxicology Program, the Department of Health and Human 
Services (including the Food and Drug Administration, the Centers for 
Disease Control and Prevention, the National Institutes of Health), the 
Occupational Health and Safety Administration, the Environmental 
Protection Agency, other federal agencies and programs, and other 
organizations concerned with reducing the risk to consumers from 
exposure to consumer product hazards. The Directorate is responsible for 
managing and safeguarding confidential business information received 
from the Environmental Protection Agency in accordance with the 
requirements of that agency.

[64 FR 66580, Nov. 29, 1999]



Sec. 1000.29  Directorate for Economic Analysis.

    The Directorate for Economic Analysis, which is managed by the 
Associate Executive Director for Economic Analysis, is responsible for 
providing the Commission with advice and information on economic and 
environmental matters and on the economic, social and environmental 
effects of Commission actions. It analyzes the potential effects of CPSC 
actions on consumers and on industries, including effects on competitive 
structure and commercial practices. The Directorate acquires, compiles, 
and maintains economic data on movements and trends in the general 
economy and on the production, distribution, and sales of consumer 
products and their components to assist in the analysis of CPSC 
priorities, policies, actions, and rules. It plans and carries out 
economic surveys of consumers and industries. It studies the costs of 
accidents and injuries. It evaluates the economic, societal, and 
environmental impact of product safety rules and standards. It performs 
regulatory analyses and studies of costs

[[Page 15]]

and benefits of CPSC actions as required by the Consumer Product Safety 
Act, The National Environmental Policy Act, the Regulatory Flexibility 
Act and other Acts, and by policies established by the Consumer Product 
Safety Commission. The Directorate manages hazard assessment and 
reduction projects as assigned.

[56 FR 30496, July 3, 1991. Redesignated at 59 FR 66673, Dec. 28, 1994, 
and further redesignated at 64 FR 66579, Nov. 29, 1999]



Sec. 1000.30  Directorate for Engineering Sciences.

    The Directorate for Engineering Sciences, which is managed by the 
Associate Executive Director for Engineering Sciences, is responsible 
for developing technical policy for and implementing the Commission's 
engineering programs. The Directorate manages hazard assessment and 
reduction projects as assigned by the Office of Hazard Identification 
and Reduction; provides engineering technical support and product safety 
assesments for the Office of Compliance; provides engineering, 
scientific, and technical expertise to the Commission and Commission 
staff as requested; and provides engineering technical support to other 
Commission organizations, activities, and programs as needed. The 
Directorate develops and evaluates product safety standards, product 
safety tests and test methods, performance criteria, design 
specifications, and quality control standards for consumer products, 
based on engineering and scientific methods. It conducts engineering 
analysis and testing of the safety of consumer products, and evaluates 
and participates in the development of mandatory and voluntary standards 
for consumer products including engineering and human factors analyses 
in support of standards development and product compliance testing. The 
Directorate performs or monitors research for consumer products in a 
broad array of engineering disciplines including chemical, electrical, 
fire protection, human factors, and mechanical engineering. It conducts 
and coordinates engineering research, testing, and evaluation activities 
with other federal agencies, private industry, and consumer interest 
groups. The Directorate conducts human factors studies and research of 
consumer product related injuries, including evaluations of labels, 
signs and symbols, instructions, and other measures intended to address 
the human component of injury prevention. The Directorate provides 
technical supervision and direction of engineering activities including 
tests and analyses conducted in the field.

[61 FR 1708, Jan. 23, 1996. Redesignated at 64 FR 66579, Nov. 29, 1999]



Sec. 1000.31  Directorate for Laboratory Sciences.

    The Directorate for Laboratory Sciences, which is managed by the 
Associate Executive Director for Laboratory Sciences, is responsible for 
conducting engineering analyses and testing of consumer products, 
supporting the development of voluntary and mandatory standards, and 
supporting the Agency's compliance activities through product safety 
assessments. A wide variety of products are tested and evaluated to 
determine the causes of failure and the hazards presented. Product 
safety tests involve mechanical, electrical, and combustion engineering, 
as well as thermal and chemical analyses. Test protocols are developed, 
test fixtures and setups are designed and fabricated, and tests are 
conducted following the requirements and guidance of voluntary and 
mandatory standards and/or using sound engineering and scientific 
judgment. The Laboratory participates with and supports other agency 
directorates on multi-disciplinary teams in the development of voluntary 
and mandatory standards. The Laboratory coordinates and cooperates with 
other Federal agencies, private industry, and consumer interest groups 
by sharing engineering and scientific research, test, and evaluation 
expertise. Additionally, Corrective Action Plans, proposed by 
manufacturers to correct a product defect, are tested and evaluated to 
assure that the proposed changes adequately resolve the problem. 
Regulated products, such as children's products, sleepwear, and bicycle 
helmets, are routinely tested and evaluated for compliance with the 
Consumer Product Safety Act, the Federal Hazardous Substances Act, the 
Flammable Fabrics

[[Page 16]]

Act, and the Poison Prevention Packaging Act. The Directorate is 
composed of the Mechanical Engineering Division, the Electrical 
Engineering Division (which includes flammable fabrics), and the 
Chemical Division. Overall, the directorate provides engineering, 
scientific, and other technical expertise to all entities within the 
Consumer Product Safety Commission.

[65 FR 53167, Sept. 1, 2000]



Sec. 1000.32  Directorate for Administration.

    The Directorate for Administration, which is managed by the 
Associate Executive Director for Administration, is responsible for 
formulating general administrative policies supporting the Commission in 
the areas of financial management, procurement, and general 
administrative support services including property and space management, 
physical security, printing, and warehousing. The Directorate is 
responsible for the payment, accounting, and reporting of all 
expenditures within the Commission and for operating and maintaining the 
Commission's accounting system and subsidiary Management Information 
System which allocates staff work time and costs to programs and 
projects.

[61 FR 1708, Jan. 23, 1996]



Sec. 1000.33  Directorate for Field Operations.

    (a) The Directorate for Field Operations, which is managed by the 
Associate Executive Director for Field Operations, has direct line 
authority over all Commission field operations; develops, issues, 
approves, or clears proposals and instructions affecting the field 
activities; and provides a central point within the Commission from 
which Headquarters officials can obtain field support services. The 
Directorate provides direction and leadership to the Regional Center 
Directors and to all field employees and promulgates policies and 
operational guidelines which form the framework for management of 
Commission field operations. The Directorate works closely with the 
other Headquarters functional units, the Regional Centers, and other 
field offices to assure effective Headquarters-field relationships, 
proper allocation of resources to support Commission priorities in the 
field, and effective performance of field tasks. It represents the field 
and prepares field program documents. It coordinates direct contact 
procedures between Headquarter's offices and Regional Centers. The 
Directorate is also responsible for liaison with State, local, and other 
Federal agencies on product safety programs in the field.
    (b) Regional Centers are responsible for carrying out investigative, 
compliance, and consumer information and public affairs activities 
within their areas. They encourage voluntary industry compliance with 
the laws and regulations administered by the Commission, identify 
product related incidents and investigate selected injuries or deaths 
associated with consumer products, and implement wide-ranging public 
information and education programs designed to reduce consumer product 
injuries. They also provide support and maintain liaison with components 
of the Commission, other Regional Centers, and appropriate Federal, 
State, and local government offices.

[56 FR 30496, July 3, 1991. Redesignated at 59 FR 66673, Dec. 28, 1994]



PART 1009--GENERAL STATEMENTS OF POLICY OR INTERPRETATION--Table of Contents




Sec.
1009.3 Policy on imported products, importers, and foreign 
          manufacturers.
1009.8 Policy on establishing priorities for Commission action.
1009.9 Policy regarding the granting of emergency exemptions from 
          Commission regulations.



Sec. 1009.3  Policy on imported products, importers, and foreign manufacturers.

    (a) This policy states the Commission's views as to imported 
products subject to the Consumer Product Safety Act (15 U.S.C. 2051) and 
the other Acts the Commission administers: The Federal Hazardous 
Substances Act (15 U.S.C. 1261), the Flammable Fabrics Act (15 U.S.C. 
1191), the Poison Prevention Packaging Act (15 U.S.C. 1471), and the 
Refrigerator Safety Act (15 U.S.C.

[[Page 17]]

1211). Basically, the Policy states that in order to fully protect the 
American consumer from hazardous consumer products the Commission will 
seek to ensure that importers and foreign manufacturers, as well as 
domestic manufacturers, distributors, and retailers, carry out their 
obligations and responsibilities under the five Acts. The Commission 
will also seek to establish, to the maximum extent possible, uniform 
import procedures for products subject to the Acts the Commission 
administers.
    (b) The Consumer Product Safety Act recognizes the critical position 
of importers in protecting American consumers from unreasonably 
hazardous products made abroad and accordingly, under that Act, 
importers are made subject to the same responsibilities as domestic 
manufacturers. This is explicitly stated in the definition of 
``manufacturer'' as any person who manufacturers or imports a consumer 
product (Section 3(a)(4); 15 U.S.C. 2052(a)(4)).
    (c) The Federal Hazardous Substances Act (15 U.S.C. 1261 et seq.), 
the Flammable Fabrics Act (15 U.S.C. 1191 et seq.), the Poison 
Prevention Packaging Act (15 U.S.C. 1471 et seq.), which were 
transferred to the jurisdiction of the Consumer Product Safety 
Commission under its enabling act, all assign responsibilities to 
importers comparable to those of manufacturers and distributors.
    (d) Historically, foreign-made products entering the United States 
were ``cleared'' by those agencies with particular jurisdiction over 
them. Products so cleared were limited in number relative to total 
imports. The Consumer Product Safety Commission has jurisdiction over a 
far larger number of products entering the United States through over 
300 ports of entry. In addition, the total number of imports has 
dramatically increased over the years and modern technology has brought 
air transport and containerized freight for rapid handling and 
distribution of consumer and other products. For the Commission to 
effectively ``clear'' such products through ports of entry could 
seriously impede and delay the transport of consumer products and impose 
additional costs to both the consumer and the importer.
    (e) The Consumer Product Safety Act provides alternative means to 
both assure the consumer safe products and facilitate the free movement 
of consumer products in commerce. For example, it requires certification 
by manufacturers (foreign and domestic), importers and private labelers 
of products that are subject to a consumer product safety standard. Such 
certification must be based on a test of each product or upon a 
reasonable testing program. The other acts enforced by the Commission do 
not specifically require certificates; however, both the Flammable 
Fabrics Act and the Federal Hazardous Substances Act encourage 
guarantees of compliance by protecting from criminal prosecution persons 
who have in good faith received such guarantees (15 U.S.C. 1197(a); 16 
CFR 302.11; 15 U.S.C. 1264(b)).
    (f) In the interest of giving the American consumer the full measure 
of protection from hazardous products anticipated by the Congress, it is 
the Commission's policy to assure that importers and foreign 
manufacturers carry out their responsibilities under all laws 
administered by this Commission. Specifically:
    (1) Importers have responsibilities and obligations comparable to 
those of domestic manufacturers. Rules and regulations promulgated by 
the Commission will reflect these responsibilities and obligations.
    (2) In promulgating its rules and regulations, the Commission 
encourages the participation and comments of the import community, 
including importers and foreign manufacturers.
    (3) All imported products under the jurisdiction of the Consumer 
Product Safety Commission shall, to the maximum extent possible, be 
subject to uniform import procedures. The Commission recognizes the need 
to establish and implement procedures that minimize delay and expense 
involved in inspecting cargo at a port of entry. The Commission 
encourages cooperation between importers, foreign manufacturers and 
foreign governments, which increases the safety of the consumer and 
facilitates the free movement of goods between countries.
    (4) When enforcement actions are appropriate, they will be directed 
toward

[[Page 18]]

the responsible officials of any import organization and will not be 
restricted to action solely against the product.
    (5) Legal actions sought by the Commission will usually be primarily 
directed toward the owner or consignee of imported goods rather than 
against the customs broker even though his or her name may appear as the 
importer of record. However, the Commissioner believes it will not serve 
the public interest to impede the Commission's rights of investigation 
and enforcement by exempting a customs broker from the coverage of the 
law merely because of his or her title or usual form of business. It may 
be relevant that a customs broker, who does not have an ownership 
interest in the goods but who is acting as an agent for the actual owner 
or consignee, signs the entry documents as importer of record. What 
effect and possible need for inclusion this will have in a particular 
case can be judged by the Commission on a case-by-case basis.
    (6) Commission procedures on imports shall be developed in the 
context of the overall responsibilities, authorities, priorities, 
resources, and compliance philosophy of this Commission. Any existing 
procedures which have been inherited from predecessor agencies will be 
reviewed and revised, if necessary, to be consistent with the authority 
and philosophy of this Commission.
    (g) The Commission recognizes that the importer may not be the only 
person to be held responsible for protecting American Consumers from 
unreasonably hazardous products made abroad, but the importer is, at 
least, in a strategic position to guarantee the safety of imported 
products.
    (h) Whenever, in the application of this policy, it appears that 
barriers to free trade may arise, the Commission may consider exceptions 
to this policy insofar as it can be done without compromising the 
Commission's responsibilities to assure safe products to the consumer.
    (i) Whenever, in the application of this policy, it appears that 
administrative or procedural aspects of the Commission's regulations are 
unduly burdening the free flow of goods, the Commission may consider 
modifications which alleviate such burdens. However, the Commission 
cannot consider any modifications which do not assure the consumer the 
same protection from unsafe foreign goods as from unsafe domestic goods.

(Sec. 9, 15 U.S.C. 1198, 67 Stat. 114; Sec. 14, 15 U.S.C. 1273, 74 Stat. 
379; 80 Stat. 1304, 1305; Sec. 17, 15 U.S.C. 2066, 86 Stat. 1223)

[40 FR 47486, Oct. 9, 1975, as amended at 41 FR 47915, Nov. 1, 1976]



Sec. 1009.8  Policy on establishing priorities for Commission action.

    (a) This document states the Consumer Product Safety Commission's 
policy on establishing priorities for action under the five acts the 
Commission administers. The policy is issued pursuant to sections 
4(f)(2) and 4(f)(3) of the Consumer Product Safety Act, as amended, and 
in further implementation of the Commission's statement of policy dated 
September 21, 1973.
    (b) It is the general policy of the Commission that priorities for 
Commission action will be established by a majority vote of its members. 
The policy will be reflected by votes on all requests for 
appropriations, an annual operating plan, and any revisions thereof. 
Recognizing that these documents are the result of a lengthy planning 
process, during which many decisions are made that substantially 
determine the content of the final documents, the Chairman shall 
continually keep the Commission apprised of, and seek its guidance 
concerning, significant problems, policy questions and alternative 
solutions throughout the planning cycle leading to the development of 
budget requests and operating plans.
    (1) Requests for appropriations. Requests for appropriations are 
submitted concurrently to the President or the Office of Management and 
Budget and to the Congress pursuant to section 27(k)(1) of the Consumer 
Product Safety Act.
    (2) Annual operating plan. The operating plan shall be as specific 
as possible with regard to products, groups of products, or generic 
hazards to be addressed. It shall be submitted to the Commission for 
approval at least 30 days prior to the beginning of the fiscal year.

[[Page 19]]

    (c) In establishing and revising its priorities, the Commission will 
endeavor to fulfill each of its purposes as set forth in section 2(b) of 
the Consumer Product Safety Act. In so doing, it will apply the 
following general criteria:
    (1) Frequency and severity of injuries. Two major criteria in 
determining priorities are the frequency and severity of injuries 
associated with consumer products. All available data including the 
NEISS hazard index and supplementary data collection systems, such as 
fire surveys and death certificate collection, shall be used to attempt 
to identify the frequency and severity of injuries. Consideration shall 
also be given to areas known to be undercounted by NEISS and a judgment 
reached as to the probable frequency and severity of injuries in such 
areas. The judgment as to severity shall include an evaluation of the 
seriousness of the injury.
    (2) Causality of injuries. Consideration shall then be given to the 
amenability of a product hazard to injury reduction through standard 
setting, information and education, or other Commission action. This 
step involves an analysis of the extent to which the product and other 
factors such as consumer behavior are causally related to the injury 
pattern. Priority shall be assigned to products according to the extent 
of product causality involvement and the extent of injuries that can 
reasonably be expected to be reduced or eliminated through commission 
action.
    (3) Chronic illness and future injuries. Certain products, although 
not presently associated with large numbers of frequent or severe 
injuries, deserve priority attention if there is reason to believe that 
the products will in the future be associated with many such injuries. 
Although not as susceptible to measurements as other product related 
injuries and illnesses, these risks shall be evaluated on the basis of 
the best information available and given priority on the basis of the 
predicted future illnesses and injuries and the effectiveness of 
Commission action in reducing or eliminating them.
    (4) Cost and benefit of CPSC action. Consideration shall be given on 
a preliminary basis to the prospective cost of Commission action to 
consumers and producers, and to the benefits expected to accrue to 
society from the resulting reduction of injuries. Consideration of 
product cost increases will be supplemented to the extent feasible and 
necessary by assessments of effects on utility or convenience of the 
product; product sales and shifts to substitutes; and industry supply 
factors, competitive structure, or employment. While all these facets of 
potential social ``cost'' cannot be subsumed in a single, quantitative 
cost measure, they will be weighed, to the extent they are available, 
against injury reduction benefits. The benefit estimates will be based 
on (i) explicitly stated expectations as to the effectiveness of 
regulatory options (derived from criterion (2), ``causality of 
injuries''); (ii) costs of injuries and deaths based on the latest 
injury cost data and analyses available to the Commission; (iii) 
explicit estimates or assumptions as to average product lives; and (iv) 
such other factors as may be relevant in particular cases. The 
Commission recognizes that in analyzing benefits as well as costs there 
will frequently be modifying factors--e.g., criteria (5) and (6)--or 
analytical uncertainties that complicate matters and militate against 
reliance on single numerical expressions. Hence the Commission cannot 
commit itself to priorities based solely on the preliminary cost/benefit 
comparisons that will be available at the stage of priority setting, nor 
to any one form of comparison such as net benefits or cost-benefit 
ratios. Commission costs will also be considered. The Commission has a 
responsibility to insure that its resources are utilized efficiently. 
Assuming other factors to be equal, a higher priority will be assigned 
to those products which can be addressed using fewer Commission 
resources.
    (5) Unforeseen nature of the risk. Other things being equal, 
consideration should be to the degree of consumer awareness both of the 
hazard and of its consequences. Priority could then be given to 
unforeseen and unforeseeable risks arising from the ordinary use of a 
product.
    (6) Vulnerability of the population at risk. Children, the elderly, 
and the handicapped are often less able to judge or escape certain 
dangers in a

[[Page 20]]

consumer product or in the home environment. Because these consumers 
are, therefore, more vulnerable to danger in products designed for their 
special use or frequently used by them, the Commission will usually 
place a higher priority, assuming other factors are equal, on preventing 
product related injury to children, the handicapped, and senior 
citizens.
    (7) Probability of exposure to hazard. The Commission may also 
consider several other things which can help to determine the likelihood 
that a consumer would be injured by a product thought to be hazardous. 
These are the number of units of the product that are being used by 
consumers, the frequency with which such use occurs, and the likelihood 
that in the course of typical use the consumer would be exposed to the 
identified risk of injury.
    (8) Additional criteria. Additional criteria may arise that the 
staff believes warrant the Commission's attention. The Commission 
encourages the inclusion of such criteria for its consideration in 
establishing priorities. The Commission recognizes that incontrovertible 
data related to the criteria identified in this policy statement may be 
difficult to locate or develop on a timely basis. Therefore, the 
Commission may not require extensive documentation on each and every 
criterion before making a decision. In addition, the Commission 
emphasizes that the order of listing of the criteria in this policy is 
not intended to indicate either the order in which they are to be 
considered or their relative importance. The Commission will consider 
all the criteria to the extent feasible in each case, and as 
interactively or jointly as possible.

(Sec. 4, 15 U.S.C. 2053, 86 Stat. 1210; as amended by sec. 4, Pub. L. 
94-284)

[42 FR 53953, Oct. 4, 1977]



Sec. 1009.9  Policy regarding the granting of emergency exemptions from Commission regulations.

    (a) This document states the Consumer Product Safety Commission's 
policy with respect to emergency requests for exemptions for companies 
which inadvertently produce products that do not conform to Commission 
regulations issued under the five acts the Commission administers. These 
acts are the Consumer Product Safety Act, the Federal Hazardous 
Substances Act, the Flammable Fabrics Act, the Poison Prevention 
Packaging Act of 1970 and the Refrigerator Safety Act. While the 
Commission is reluctant to grant such requests, it believes that the 
public should be apprised of the manner in which it rules on exemption 
requests and therefore is publishing the policy to provide guidance to 
industry and others making such requests. The publication of the policy 
will also serve to inform the public of the criteria that the Commission 
uses in ruling upon such requests. This policy is intended to cover 
emergency requests for exemptions and, while relevant, is not intended 
to limit the discretion of CPSC staff to close or not to open cases in 
the routine enforcement of CPSC regulations.
    (b) The policy governs requests for exemption from any regulation 
under any act the Commission administers. The policy lists criteria the 
Commission considers in deciding whether to grant or deny an exemption 
request and therefore, should provide guidance to companies on the types 
of information to be submitted with requests. In addition, published 
Commission procedures regarding petitioning for amendments to 
regulations may assist companies in determining what supporting data to 
submit with a request. (See, for example, existing Commission procedures 
at 16 CFR 1110, 16 CFR 1607.14, 16 CFR 1500.82 and 16 CFR 1500.201). The 
exemption requests themselves should be filed with the Office of the 
Secretary of the Commission.
    (c) It is the general policy of the Commission that when a 
particular exemption request is made and granted, all similarly situated 
persons are accorded the same relief as the person who requested the 
exemption. Therefore, when any amendment to a Commission regulation is 
proposed or a statement of enforcement policy is issued, the document to 
the extent practicable will be phrased in objective terms so that all 
similarly situated persons will be able to determine whether their 
products would fall within the relief.

[[Page 21]]

    (d) In deciding whether to grant or deny an exemption request, the 
Commission considers the following general criteria:
    (1) The degree to which the exemption if granted would expose 
consumers to an increased risk of injury: The Commission does not 
believe it should exempt products which would present a significantly 
greater risk to consumers than complying products. Therefore, the 
Commission will not grant exemption requests in such cases.
    (2) The cost to the Commission of granting emergency requests: 
Granting emergency exemption requests will in most cases require 
drafting a proposed and a final amendment or a statement of enforcement 
policy for publication in the Federal Register. Such action may also 
require the Commission to monitor the sale or distribution of the 
products. These activities consume scarce Commission resources. In some 
instances, the costs to the Commission may exceed the benefit to be 
derived by a company and similarly situated companies. If so, the 
Commission may deny the request on this ground.
    (3) The precedential effect of exempting some products: The 
Commission recognizes that decisions to exempt some products set 
precedents in at least two ways. First, they indicate to companies that 
the CPSC will permit deviations to a given regulation. Second, they 
indicate to companies that the CPSC will permit deviations to 
regulations in general. Both precedents, if set carelessly by the CPSC, 
could result in many requests for exemption and could undermine the 
stability and integrity of the Commission's regulations.
    (e) In deciding whether to grant or deny an exemption request, the 
Commission also considers the following factors which relate 
specifically to the company making the request: (If the request is 
granted, all similarly situated companies, however, will be accorded the 
same relief).
    (1) The nature of the emergency exemption request: The Commission 
will not reward bad quality control or faulty design work by permitting 
companies to market their mistakes. Although it is difficult to detail 
specific instances, the Commission is sympathetic to companies that 
produced noncomplying products due to factors beyond their immediate 
control or despite their best efforts.
    (2) The economic loss which a company will suffer if its emergency 
request is denied: The greater the loss a company may suffer the more 
likely the Commission will favorably consider an exemption. However, the 
Commission does not believe economic loss alone should be determinative 
of an emergency exemption request.
    (3) The fairness to competitors: The Commission is reluctant to 
grant relief if it could place the company at an unfair competitive 
advantage over other companies which have successfully complied with the 
same regulation. Therefore, the Commission will afford the same relief 
to similarly situated companies, and will decline to grant a request 
where unfair competitive advantage may result.

(15 U.S.C. 1191, 1261, 1471, 2051, 2111)

[44 FR 40639, July 12, 1979]

                          PART 1010 [RESERVED]



PART 1011--NOTICE OF AGENCY ACTIVITIES--Table of Contents




Sec.
1011.1 General policy considerations; scope.
1011.2 Definitions.
1011.3 General requirements for various kinds of meetings.
1011.4 Forms of advance public notice of meetings; Public Calendar/
          Master Calendar and Federal Register.

    Authority: 5 U.S.C. 552b(g); Pub. L. 92-573, 86 Stat. 1207 (15 
U.S.C. 2051-81) as amended by Pub. L. 94-284, 90 Stat. 503, Pub. L. 95-
319, 92 Stat. 386, Pub. L. 95-631, 92 Stat. 3742; Pub. L. 90-189, 81 
Stat. 568 (15 U.S.C. 1191-1204); Pub. L. 86-613, 74 Stat. 372, as 
amended by Pub. L. 89-756, 80 Stat. 1303, and Pub. L. 91-113, 83 Stat. 
187 (15 U.S.C. 1261-74); Pub. L. 91-601, 84 Stat. 1670 (15 U.S.C. 1471-
76) and the Act of Aug. 7, 1956, 70 Stat. 953 (15 U.S.C. 1211-14).

    Source: 46 FR 38322, July 24, 1981, unless otherwise noted.



Sec. 1011.1  General policy considerations; scope.

    (a) In order for the Consumer Product Safety Commission to properly 
carry out its mandate to protect the

[[Page 22]]

public from unreasonable risks of injury associated with consumer 
products, the Commission has determined that it must involve the public 
in its activities to the fullest possible extent.
    (b) To ensure public confidence in the integrity of Commission 
decisionmaking, the Agency, to the fullest possible extent, will conduct 
its business in an open manner free from any actual or apparent 
impropriety.
    (c) This part 1011 presents general provisions concerning public 
notice for various types of Agency activities.



Sec. 1011.2  Definitions.

    As used in this part 1011, the following terms shall have the 
meanings set forth:
    (a) Agency. The entire organization which bears the title Consumer 
Product Safety Commission (CPSC).
    (b) Agency staff. Employees of the Agency other than the five 
Commissioners.
    (c) Commissioner. An individual who belongs to the collegial body 
heading the CPSC.
    (d) Commission. The Commissioners of the Consumer Product Safety 
Commission acting in an official capacity.
    (e) Commission Meeting. A meeting of the Commissioners subject to 
the Government in the Sunshine Act, 5 U.S.C. 552b. This term is more 
fully defined in the Commission's regulations under the Government in 
the Sunshine Act, 16 CFR part 1013.
    (f) Agency meeting. A meeting between Agency personnel, including 
individual Commissioners, and outside parties. This term and the term 
``outside party'' are more fully defined in the Commission's Meeting 
Policy, 16 CFR part 1012.



Sec. 1011.3  General requirements for various kinds of meetings.

    Meetings which involve Agency staff or the Commissioners, other than 
Commission meetings, are classified in the following categories and 
shall be held according to the procedures outlined within each category.
    (a) Hearings. Hearings are public inquiries held by direction of the 
Commission for the purpose of fact finding or to comply with statutory 
requirements. The Office of the Secretary is responsible for providing 
transcription services at the hearings. Where possible, notice of 
forthcoming hearings will be published in the Public Calendar and the 
Federal Register at least 30 days before the date of the hearings.
    (b) Meetings between Commissioners or Agency staff and outside 
parties. The requirements for Agency meetings between Commissioners or 
Agency staff and outside parties involving substantial interest matters 
are contained in 16 CFR part 1012.
    (c) Commission meetings. The requirements for Commission meetings 
under the Government in the Sunshine Act, 5 U.S.C. 552b are contained in 
16 CFR part 1013.
    (d) Staff meetings. As a general rule, only Agency employees attend 
staff meetings. At the discretion of the participants, Staff meetings 
may be listed on the Public Calendar and attendance by the public may be 
permitted. Recordkeeping is at the discretion of the participants.
    (e) Advisory committee meetings. Meetings of the Agency's advisory 
committees are scheduled by the Commission. Advance notice will be given 
in both the Public Calendar and the Federal Register. Advisory committee 
meetings serve as a forum for discussion of matters relevant to the 
Agency's statutory responsibilities with the objective of providing 
advice and recommendations to the Commission. The Agency's advisory 
committees are the National Advisory Committee for the Flammable Fabrics 
Act, the Product Safety Advisory Council, the Technical Advisory 
Committee on Poison Prevention Packaging and the Toxicological Advisory 
Board. The Office of the Secretary is responsible for the recordkeeping 
for such meetings. The Commission's regulation for the management of its 
advisory committees is set out in 16 CFR part 1018.



Sec. 1011.4  Forms of advance public notice of meetings; Public Calendar/Master Calendar and Federal Register.

    Advance notice of Agency activities is provided so that members of 
the public may know of and participate in these activities to the 
fullest extent

[[Page 23]]

possible. Where appropriate, the Commission uses the following types of 
notice for both Agency meetings subject to 16 CFR part 1012 and 
Commission meetings subject to 16 CFR part 1013:
    (a) Public Calendar/Master Calendar. (1) The printed Public Calendar 
and the Master Calendar maintained in the Office of the Secretary are 
the principal means by which the Agency notifies the public of its day-
to-day activities. The Public Calendar and/or Master Calendar provide 
advance notice of public hearings, Commission meetings, Agency meetings 
with outside parties involving substantial interest matters, other 
Agency meetings, selected staff meetings, advisory committee meetings, 
and other activities such as speeches and participation in panel 
discussions, regardless of the location. The Public Calendar also lists 
recent CPSC Federal Register issuances and Advisory Opinions of the 
Office of the General Counsel.
    (2) Upon request in writing to the Office of the Secretary, Consumer 
Product Safety Commission, Washington, D.C. 20207, any person or 
organization will be sent the Public Calendar on a regular basis free of 
charge. In addition, interested persons may contact the Office of the 
Secretary to obtain information from the Master Calendar which is kept 
current on a daily basis.
    (3) The Public Calendar and the Master Calendar, supplemented by 
meeting summaries, are intended to serve the requirements of section 
27(j)(8) of the Consumer Product Safety Act (15 U.S.C. 2076(j)(8)).
    (b) Federal Register. Federal Register is the publication through 
which official notifications, including formal rules and regulations of 
the Agency, are made. Because the Public Calendar and/or Master Calendar 
are the primary devices through which the Agency notifies the public of 
its routine, daily activities, the Federal Register will be utilized 
only when required by the Government in the Sunshine Act (as provided in 
16 CFR part 1013) or other applicable law, or when the Agency believes 
that the additional coverage which the Federal Register can provide is 
necessary to assist in notification to the public of important meetings.



PART 1012--MEETINGS POLICY--MEETINGS BETWEEN AGENCY PERSONNEL AND OUTSIDE PARTIES--Table of Contents




Sec.
1012.1 General policy considerations; scope.
1012.2 Definitions.
1012.3 Advance public notice of agency meetings.
1012.4 Public attendance at agency meetings.
1012.5 Recordkeeping for agency meetings.
1012.6 The news media.
1012.7 Telephone conversations.

    Authority: Pub. L. 92-573, 86 Stat. 1207 (15 U.S.C. 2051-81) as 
amended by Pub. L. 94-284, 90 Stat. 503, Pub. L. 95-319, 92 Stat. 386, 
Pub. L. 95-631, 92 Stat. 3742; Pub. L. 90-189, 81 Stat. 568 (15 U.S.C. 
1191-1204); Pub. L. 86-613, 74 Stat. 372, as amended by Pub. L. 89-756, 
80 Stat. 1303, and Pub. L. 91-113, 83 Stat. 187 (15 U.S.C. 1261-74); 
Pub. L. 91-601, 84 Stat. 1670 (15 U.S.C. 1471-76) and the Act of Aug. 7, 
1956, 70 Stat. 953 (15 U.S.C. 1211-14).

    Source: 46 FR 38323, July 24, 1981, unless otherwise noted.



Sec. 1012.1  General policy considerations; scope.

    (a) To achieve its goals of involving the public in its activities 
and conducting its business in an open manner, the Agency, whenever 
practicable, shall notify the public in advance of all meetings 
involving matters of substantial interest held or attended by its 
personnel, and shall permit the public to attend such meetings. 
Furthermore, to ensure the widest possible exposure of the details of 
such meetings, the Agency will keep records of them freely available for 
inspection by the public.
    (b) This part 1012, the Agency's Meetings Policy, sets forth 
requirements for advance public notice, public attendance, and 
recordkeeping for Agency meetings.



Sec. 1012.2  Definitions.

    (a) As used in this part 1012, the following terms have the 
respective meanings set forth in paragraphs (a)-(d) of Sec. 1011.2 of 
this subchapter: ``Agency,'' ``Agency staff,'' ``Commissioner,'' 
``Commission.''
    (b) Agency meeting. Any face-to-face encounter, other than a 
Commission meeting subject to the Government in

[[Page 24]]

the Sunshine Act, 5 U.S.C. 552b, and part 1013, in which one or more 
employees, including Commissioners, discusses with an outside party any 
subject relating to the Agency or any subject under its jurisdiction. 
The term Agency meeting does not include telephone conversations, but 
see Sec. 1012.8 which relates to telephone conversations.
    (c) Outside party. Any person not an employee, not under contract to 
do work for the Agency, or not acting in an official capacity as a 
consultant to the Consumer Product Safety Commission, such as advisory 
committee members or offeror personnel. Examples of persons falling 
within this definition are representatives from industry and consumer 
groups. Members of the news media when acting in a newsgathering 
capacity are not outside parties. (See also Sec. 1012.7.) Officers and 
employees of the Federal Government when acting in their official 
capacities (except when advocating a particular course of action on 
behalf of an outside party) are not outside parties.
    (d) Substantial interest matter. Any matter, other than that of a 
trivial nature, that pertains in whole or in part to any issue that is 
likely to be the subject of a regulatory or policy decision by the 
Commission. Pending matters, i.e., matters before the Agency in which 
the Agency is legally obligated to make a decision, automatically 
constitute substantial interest matters. Examples of pending matters 
are: Scheduled administrative hearings; matters published for public 
comments; petitions under consideration; and mandatory standard 
development activities. The following are some examples of matters that 
do not constitute substantial interest matters: Inquiries concerning the 
status of a pending matter; discussions relative to general 
interpretations of existing laws, rules, and regulations; inspection of 
nonconfidential CPSC documents by the public; negotiations for 
contractual services; and routine CPSC activities such as recruitment, 
training, meetings involving consumer deputies, or meetings with 
hospital staff and other personnel involved in the National Electronic 
Injury Surveillance System.



Sec. 1012.3  Advance public notice of agency meetings.

    (a) Commissioners and Agency employees are responsible for reporting 
meeting arrangements for Agency meetings to the Office of the Secretary 
so that they may be published in the Public Calendar or entered on the 
Master Calendar at least seven days before a meeting, except as provided 
in paragraph (d) of this section. These reports shall include the 
following information:
    (1) Probable participants and their affiliations;
    (2) Date, time and place of the meeting;
    (3) Subject of the meeting (as fully and precisely described as 
possible);
    (4) Who requested the meeting;
    (5) Whether the meeting involves matters of substantial interest;
    (6) Notice that the meeting is open or reason why the meeting or any 
portion of the meeting is closed (e.g., discussion of trade secrets); 
and
    (7) Names and telephone number of the CPSC host or CPSC contact 
person.
    (b) Once a report has been made to the Office of the Secretary, 
Agency employees subsequently desiring to attend the meeting need not 
notify the Office of the Secretary.
    (c) When there is no opportunity to give seven days advance notice 
of a meeting, Agency employees (other than the Commissioners or their 
personal staff) who desire to hold or attend such a meeting must obtain 
the approval of the General Counsel or his or her designee. Requests for 
waiver of the seven-day advance notice requirement by members of the 
staff who report to the Executive Director may only be submitted to the 
General Counsel or his or her designee in writing by the Executive 
Director or his or her designee. Personal staff of Commissioners must 
obtain the approval of their respective Commissioners. If the short 
notice is approved, the Agency employee must notify the Office of the 
Secretary in advance of the meeting to record the meeting on the Master 
Calendar. The Office of the Secretary shall publish notice of the 
meeting as an addendum to the next Public Calendar.
    (d) Exceptions. The notice requirement shall not apply to:

[[Page 25]]

    (1) Meetings with outside parties not involving substantial interest 
matters (although such meetings should be limited where the public 
interest would be served);
    (2) Meetings with outside parties held during the normal course of 
surveillance, inspection, or investigation under any of the Acts 
administered by the Commission, including informal citation hearings 
under the Federal Hazardous Substance Act or the Poison Prevention 
Packaging Act;
    (3) Meetings with outside parties concerning the settlement or 
negotiation of an individual case, including proposed remedial action, 
or meetings concerning any administrative or judicial action in which 
the outside party is a participant, party, or amicus curiae;
    (4) Routine speeches given by CPSC personnel before outside parties. 
However, for information purposes, personnel are encouraged to submit 
advance notice of these speeches to the Office of the Secretary for 
inclusion in the Public Calendar;
    (5) Meetings with other Federal personnel that are also attended by 
outside parties except where a specific matter to be discussed is also 
pending before the Commission or its staff;
    (6) Meetings with state, local or foreign government personnel 
concerning intergovernmental cooperative efforts and not the advocacy of 
a particular course of action on behalf of a constituency of the 
governmental entity;
    (7) Meetings or discussions with or at the request of either members 
of Congress and their staffs relating to legislation, appropriation or 
oversight matters, or Management and Budget personnel relating to 
legislation or appropriation matters;
    (8) Pre-proposal conferences involving confidential contracts made 
pursuant to 41 U.S.C. 252(c)(12) in connection with potential litigation 
matters.



Sec. 1012.4  Public attendance at agency meetings.

    (a) Any person may attend any meeting involving a substantial 
interest matter unless that meeting has been listed as a closed meeting. 
For meetings not involving substantial interest matters, the chairperson 
of the meeting may exercise his or her discretion to allow attendance by 
a member of the public.
    (b) When meetings between Agency employees and outside parties are 
open to the public, attendance may be limited by space. When feasible, a 
person or organization desiring to attend such a meeting should give at 
least one day advance notice to one of the employees holding or 
attending the meeting so that sufficient space can be arranged for all 
those wishing to attend.
    (c) Members of the public attending Agency meetings generally may 
observe only. The chairperson of the meeting may exercise his or her 
discretion to permit members of the public to participate as well.
    (d) The following Agency meetings are not open to the public:
    (1) Meetings, or, if possible, portions of meetings where the 
General Counsel or his or her designee has determined that proprietary 
data are to be discussed in such a manner as to imperil their 
confidentiality;
    (2) Meetings held by outside parties at which limits on attendance 
are imposed by lack of space, provided that such meetings are open to 
the news media;
    (3) Meetings with outside parties held during the normal course of 
surveillance, inspection, or investigation under any of the Acts 
administered by the Commission, including informal citation hearings 
under the Federal Hazardous Substances Act or the Poison Prevention 
Packaging Act;
    (4) Meetings with outside parties concerning the settlement or 
negotiation of an individual case, including proposed remedial action, 
or meetings concerning any administrative or judicial action in which 
the outside party is a participant, party, or amicus curiae;
    (5) Meetings with other Federal personnel that are attended by 
outside parties except where a specific matter to be discussed is also 
pending before the Commission or its staff;
    (6) Meetings with state, local or foreign government personnel 
concerning intergovernmental cooperative efforts and not the advocacy of 
a particular course of action on behalf of a constituency of the 
governmental entity;
    (7)(i) Meetings between Agency staff (other than Commissioners and 
their

[[Page 26]]

personal staff) and an outside party when the General Counsel or his or 
her designee determines that extraordinary circumstances require that 
the meeting be closed. Requests for exemption by members of the staff 
who report to the Executive Director may be submitted to the General 
Counsel or his or her designee in writing only by the Executive Director 
or his or her designee. In such a case, the reasons for closing the 
meeting or a portion of the meeting shall be stated in the Public 
Calendar notice announcing the meeting;
    (ii) Meetings between a Commissioner (or his or her personal staff) 
and an outside party when, in the opinion of the Commissioner, 
extraordinary circumstances require that the meeting be closed. In such 
a case, the reasons for closing the meeting or a portion of the meeting 
must be stated in the Public Calendar notice announcing the meeting;
    (8) Meetings or discussions with or at the request of either members 
of Congress and their staffs relating to legislation, appropriation or 
oversight matters, or Management and Budget personnel relating to 
legislation or appropriation matters; and
    (9) Pre-proposal conferences involving confidential contracts made 
pursuant to 41 U.S.C. 252(c)(12), in connection with the potential 
litigation matters.



Sec. 1012.5  Recordkeeping for agency meetings.

    (a) This section describes and establishes requirements for the two 
types of records maintained for Agency meetings, Agency meeting 
summaries and transcripts.
    (b) Agency meeting summaries. Agency meeting summaries are written 
records settling forth the issues discussed at all Agency meetings with 
outside parties involving substantial interest matters. Any Commission 
employee who holds or attends an Agency meeting involving a substantial 
interest matter must prepare a meeting summary. However, only one agency 
meeting summary is required for each meeting even if more than one CPSC 
employee holds or attends the meeting. Agency meeting summaries are 
generally available to the public in the Agency's Public Reading Room in 
the Office of the Secretary as described in paragraph (b)(2) of this 
section.
    (1) An agency meeting summary should state the essence of all 
substantive matters relevant to the Agency, especially any matter 
discussed which was not listed on the Public Calendar, and should 
describe any decisions made or conclusions reached regarding substantial 
interest matters. An agency meeting summary should also indicate the 
date of the meeting and the identity of persons who attended.
    (2) An agency meeting summary or a notice of cancellation of the 
meeting must be submitted to the Office of the Secretary within twenty 
(20) calendar days after the meeting for which the summary is required. 
The Office of the Secretary shall maintain a file of the meeting 
summaries in chronological order, which shall be available to the public 
to the extent permitted by law.
    (c) Transcripts. Transcripts are generally taken at public hearings 
and certain Agency meetings when complex subjects indicate verbatim 
records are desirable. The transcript may also include exhibits 
submitted to be part of the formal record of an Agency meeting. Copies 
of such transcripts are placed on file for public inspection in the 
Office of the Secretary.



Sec. 1012.6  The news media.

    The Agency recognizes that the news media occupy a unique position 
in informing the public of the Agency's activities. The Commission 
believes that the inherently public nature of the news media allows 
their activities to be exempt from the requirements of this part 
whenever Agency meetings are held with the news media for the purpose of 
informing them about Agency activities. Such Agency meetings are not 
exempt in the event that any representative of the news media attempts 
to influence any Agency employee on a substantial interest matter.



Sec. 1012.7  Telephone conversations.

    (a) Telephone conversations present special problems regarding 
Agency meetings. The Commission recognizes that persons outside the 
Agency have a

[[Page 27]]

legitimate right to receive information and to present their views 
regarding Agency activities. The Commission also recognizes that such 
persons may not have the financial means to travel to meet with Agency 
employees. However, because telephone conversations, by their very 
nature, are not susceptible to public attendance, or participation, 
Agency employees must take care to ensure that telephone conversations 
are not utilized to circumvent the provisions of this part.
    (b) Two basic rules apply to telephone conversations:
    (1) Any Agency employee holding a telephone conversation in which 
substantial interest matters are discussed with an outside party must 
prepare a telephone call summary of the conversation. The summary must 
meet the requirements of Sec. 1012.5(b), and must be submitted to the 
Office of the Secretary within twenty (20) calendar days of the 
conversation. The Office of the Secretary shall maintain file of 
telephone call summaries in chronological order which shall be available 
to the public to the extent permitted by law.
    (2) All Agency employees must exercise sound judgment in discussing 
substsantial interest matters during a telephone conversation. In the 
exercise of such discretion Agency employees should not hesitate to 
terminate a telephone conversation and insist that the matters being 
discussed be postponed until an Agency meeting with appropriate advance 
public notice may be scheduled, or, if the outside party is financially 
or otherwise unable to meet with the Agency employee, until the matter 
is presented to the Agency in writing.



PART 1013--GOVERNMENT IN THE SUNSHINE ACT, RULES FOR COMMISSION MEETINGS--Table of Contents




Sec.
1013.1 General policy considerations; scope.
1013.2 Definitions.
1013.3 Announcement of Commission meetings and changes after 
          announcement.
1013.4 Public attendance at Commission meetings.
1013.5 Recordkeeping requirements.
1013.6 Public availability of transcripts, recordings and minutes of 
          Commission meetings.

    Authority: 5 U.S.C. 552b(g).

    Source: 46 FR 38326, July 24, 1981, unless otherwise noted.



Sec. 1013.1  General policy considerations; scope.

    (a) In enacting the Government in the Sunshine Act, 5 U.S.C. 552b, 
the Congress stated the policy that, to the fullest practicable extent, 
the public is entitled to information regarding the decisionmaking 
processes of the Federal Government. The purpose of the Government in 
the Sunshine Act is to provide the public with such information while 
protecting both the rights of individuals and the ability of the 
Government to carry out its responsibilities. When the Commissioners of 
the Consumer Product Safety Commission hold meetings for the purpose of 
jointly conducting or disposing of Commission business they will conduct 
these meetings in accordance with the provisions of the Government in 
the Sunshine Act.
    (b) This part 1013 prescribes rules the Commission follows in 
carrying out the Government in the Sunshine Act.



Sec. 1013.2  Definitions.

    (a) As used in this part 1013, the following terms shall have the 
respective meanings set forth in paragraphs (a), (c) and (d) of 
Sec. 1011.2 of this subchapter: ``Agency,'' ``Commissioner,'' 
``Commission.''
    (b) Majority of the Commission. Three or more of the Commissioners.
    (c) Commission meeting. The joint deliberations of at least a 
majority of the Commission where such deliberations determine or result 
in the joint conduct or disposition of official Agency business. This 
term does not include meetings required or permitted by Sec. 1013.4(b) 
(to determine whether a meeting will be open or closed), meetings 
required or permitted by Sec. 1013.3(e) (to change the subject matter of 
a meeting or the determination to open or close a meeting after the 
public announcement) or meetings required or permitted by 1013.3(c) (to 
dispense with the one week advance notice of a meeting).

[[Page 28]]



Sec. 1013.3  Announcement of Commission meetings and changes after announcement.

    (a) The Secretary of the Commission is responsible for preparing and 
making public the announcements and notices relating to Commission 
meetings that are required in this part.
    (b) The Agency shall announce each Commission meeting in the Public 
Calendar or Master Calendar at least one week (seven calendar days) 
before the meeting. The Agency shall concurrently submit the 
announcement for publication in the Federal Register. The announcement 
and the Federal Register notice shall contain the following information:
    (1) The date, time, and place of the meeting;
    (2) The subject matter of the meeting;
    (3) Whether the meeting will be open or closed to the public;
    (4) The name and phone number of the official who responds to 
requests for information about the meeting.
    (c) If a majority of the Commission determines by recorded vote that 
Agency business requires calling a meeting without seven calendar days 
advance public notice, the Office of the Secretary shall announce this 
determination in the Public Calendar or Master Calendar at the earliest 
practicable time and shall concurrently transmit the announcement for 
publication in the Federal Register.
    (d) When necessary and at the direction of the Chairman, the 
Secretary shall change the time of a Commission meeting after the 
announcement in the Public Calendar or Master Calendar. Any such change 
shall be entered on the Master Calendar and such other notice shall be 
given as is practicable.
    (e) After announcement of a Commission meeting in the Public 
Calendar or Master Calendar, the Commission may change the subject 
matter of a Commission meeting or the decision to open or close a 
Commission meeting or portion thereof to the public, only if a majority 
of the Commission determines by recorded vote that Agency business so 
requires, and only if a majority of the Commission determines by 
recorded vote that no earlier announcement of the change was possible. 
The Commission shall announce the change in the Public Calendar or 
Master Calendar at the earliest practicable time before the meeting and 
shall concurrently transmit the announcement for publication in the 
Federal Register. Announcement of the change shall include the vote of 
each Commissioner upon the change. (See also Sec. 1013.4(d) for 
requirements for Commission reconsideration of a decision to open or 
close a meeting to the public.)



Sec. 1013.4  Public attendance at Commission meetings.

    (a) Attendance by the public. Every portion of every Commission 
meeting shall be open to public observation except as provided in 
paragraph (b) of this section. Notwithstanding the applicability of the 
exemptions contained in paragraph (b) of this section, a Commission 
meeting or portions thereof shall be open to public observation when the 
Commission determines that the public interest so requires. The 
Commission shall take into account in all cases the relative advantages 
and disadvantages to the public of conducting the Commission meeting in 
open session. The number of public observers shall be limited only by 
availability of space. Attendance by the public shall usually be limited 
to observation and shall not include participation except where, by 
majority vote, the Commission determines that data or views from certain 
members of the public will be permitted. To the extent their use does 
not interfere with the conduct of open meetings, cameras and sound-
recording equipment may be used at open Commission meetings. The 
Chairman or presiding Commissioner shall insure that use of such 
equipment does not disrupt the meeting.
    (b) Exemptions to the requirement of openness. The requirement in 
paragraph (a) of this section that all Commission meetings be open to 
public observation shall not apply to any Commission meeting or portion 
thereof for which the Commission has determined in accordance with the 
procedures for closing meetings set forth in paragraph (c) of this 
section, that such meeting or portion thereof is likely to:

[[Page 29]]

    (1) Disclose matters that are specifically authorized under criteria 
established by an Executive Order to be kept secret in the interest of 
national defense or foreign policy and in fact are properly classified 
pursuant to such Executive Order;
    (2) Relate solely to the internal personnel rules and practices of 
the Agency;
    (3) Disclose matters specifically exempted from disclosure by 
statute (other than 5 U.S.C. 552): Provided, That such statute (i) 
requires that the matters be withheld from the public in such a manner 
as to leave no discretion on the issue, or (ii) establishes particular 
criteria for withholding or refers to particular types of matters to be 
withheld;
    (4) Disclose trade secrets and commercial or financial information 
obtained from a person and privileged or confidential;
    (5) Involve accusing any person of a crime, or formally censuring 
any person;
    (6) Disclose information of a personal nature where disclosure would 
constitute a clearly unwarranted invasion of personal privacy;
    (7) Disclose investigatory records compiled for law enforcement 
purposes or information which if written would be contained in such 
records, but only to the extent that the production of such records or 
information would,
    (i) Interfere with enforcement proceedings,
    (ii) Deprive a person of a right to a fair trial or an impartial 
adjudication,
    (iii) Constitute an unwarranted invasion of personal privacy,
    (iv) Disclose the identity of a confidential source and, in the case 
of a record compiled by a criminal law enforcement authority in the 
course of a criminal investigation, or by an agency conducting a lawful 
national security intelligence investigation, confidential information 
furnished only by the confidential source,
    (v) Disclose investigative techniques and procedures or,
    (vi) Endanger the life or physical safety of law enforcement 
personnel;
    (8) Disclose information contained in or related to examination, 
operating or condition reports prepared by, on behalf of, or for the use 
of an agency responsible for the regulation or supervision of financial 
institutions;
    (9) Disclose information the premature disclosure of which would be 
likely to significantly frustrate implementation of a proposed Agency 
action. This provision does not apply in any instance where the Agency 
has already disclosed to the public the content or nature of its 
proposed action, or where the Agency is required by law to make such 
disclosure on its own initiative prior to taking final agency action on 
such proposal; or
    (10) Specifically concern the Agency's issuance of a subpoena, or 
the Agency's participation in a civil action or proceeding, an action in 
a foreign court or international tribunal, or an arbitration, or the 
initiation, conduct, or disposition by the Agency of a particular case 
of formal agency adjudication pursuant to the procedures in 5 U.S.C. 554 
or otherwise involving a determination on the record after opportunity 
for a hearing.
    (c) Procedure for closing Commission Meetings. The following 
procedure shall be followed in closing a Commission meeting or portion 
thereof to public observation:
    (1) A majority of the Commission must vote to close a meeting or 
portion thereof to public observation pursuant to paragraph (b) of this 
section. A separate vote of the Commission shall be taken for each 
matter with respect to which a Commission meeting is proposed to be 
closed to public observation. Each such vote may, at the discretion of 
the Commission, apply to that portion of any meeting held within the 
following thirty days in which such matter is to be discussed. The vote 
of each Commissioner participating in such vote shall be recorded and no 
proxies shall be allowed.
    (2) Any person whose interest may be directly affected if a portion 
of a Commission meeting is open may request in writing to the Office of 
the Secretary that the Commission close that portion of the meeting on 
the basis of paragraph (b) (5), (6), or (7) of this section. The 
Commission shall vote on such requests if at least one Commissioner 
desires to do so.

[[Page 30]]

    (3) Before the Commission may hold a closed meeting the General 
Counsel must certify that in his or her opinion, the meeting may 
properly be closed to the public. Such certification shall be in writing 
and shall state each relevant exemptive provision.
    (4) Within one day of a vote in accordance with paragraph (c) (1) or 
(2) of this section to close a Commission meeting or portion thereof, 
the Secretary shall make available to the public a notice setting forth:
    (i) The results of the vote reflecting the vote of each 
Commissioner;
    (ii) A full explanation of the action of the Commission closing the 
meeting or portion thereof, including reference to the specific basis 
for such closing (see paragraph (b) of this section) and an explanation, 
(without disclosing exempt information), of why the Commission concludes 
on balance, taking into account the relative advantages and 
disadvantages to the public of conducting the meeting in open or closed 
session, that the public interest would best be served by closing the 
meeting;
    (iii) A list of all non-Agency personnel expected to attend the 
meeting and their affiliations; and
    (iv) A certification by the General Counsel that in his or her 
opinion, the meeting may properly be closed to the public. If a vote to 
close a Commission meeting takes place on the same day as the meeting, 
the certification must be made available to the public before the 
meeting is convened.
    (5) The public release of the portion of the written statement 
required by paragraph (c)(4)(ii) of this section may be delayed upon a 
determination by the Commission, by recorded vote, that such a notice, 
or portion thereof, would disclose information which may be withheld in 
accordance with paragraphs (b) (1) through (10) of this section.
    (d) Reconsideration of a decision to open or close a Commission 
meeting. The Commission may, in accordance with the procedures in 
Sec. 1013.3(3) or paragraph (c)(2) of this section, reconsider its 
decision to open or close a Commission meeting when it finds that the 
public interest so requires.

[46 FR 38326, July 24, 1981, as amended at 48 FR 36566, Aug. 12, 1983]



Sec. 1013.5  Recordkeeping requirements.

    (a) Commission meetings, transcripts, recordings, or minutes.
    (1) The Agency shall maintain a complete transcript or electronic 
recording of each Commission meeting, whether open or closed, except 
that in the case of a Commission meeting or portion thereof closed to 
the public pursuant to paragraph (b)(10) of Sec. 1013.4, the Agency may 
elect to maintain a set of meeting minutes instead of a transcript or a 
recording. Minutes of such closed Commission meetings shall:
    (i) Fully and clearly describe all matters discussed, and
    (ii) Provide a full and accurate summary of any actions taken and 
the reasons therefor, including a description of each of the views 
expressed on any item and the record of any roll call vote (reflecting 
the vote of each Commissioner on the question). All documents considered 
in connection with any action shall be identified in the meeting 
minutes.
    (2) The transcript, recording or minutes of closed Commission 
meetings shall include the certification by the General Counsel or by 
his or her designee, required by Sec. 1013.4(c)(3) and a statement by 
the presiding Commissioner setting forth the date, time and place of the 
meeting and the persons present.
    (3) The transcript, recording, or minutes of any Commission meeting 
may include attachments such as Commission opinions, briefing papers, or 
other documents presented at the meeting.
    (4) The transcript and accompanying material shall be maintained by 
the Secretary for a period of at least two years after the meeting, or 
until one year after the conclusion of any Agency proceeding with 
respect to which the meeting, or portion thereof, was held, whichever 
occurs later.
    (b) Minutes of Commission Decisions. Minutes of Commission Decisions 
summarizing the issues presented to the Commission for decision and 
indicating the vote of each Commissioner document the decisions of the 
Commission, whether made at open or closed meetings or by ballot vote. 
The Commission's final Minutes of Commission Decisions, issued by the 
Office of the Secretary, constitute the official means of

[[Page 31]]

recording the decisions of the Commission and the votes of individual 
Commissioners.



Sec. 1013.6  Public availability of transcripts, recordings and minutes of Commission meetings.

    (a) Availability of transcripts, recordings or minutes. The Agency 
shall make available to the public the transcript, recording or minutes 
of Commission meetings. However, unless the Commission finds that the 
public interest requires otherwise, any portion of the transcript, 
recording or minutes of a closed Commission meeting which is determined 
to contain information which may properly be withheld from the public on 
the basis of paragraphs (b) (1) through (10) of Sec. 1013.4 need not be 
made available to the public.
    (b) Procedures for making available transcripts, recordings or 
meeting minutes. Meeting records will be made available for inspection, 
or copies will be furnished, as requested, in accordance with the 
following procedures.
    (1) Requests. Requests for inspection or copies shall be in writing 
addressed to the Secretary, Consumer Product Safety Commission, 
Washington, D.C. 20207. A request must reasonably describe the 
Commission meeting, or portion thereof, including the date and subject 
matter or any other information which may help to identify the requested 
material.
    (2) Responses to requests. The responsibility for responding to 
requests for meeting records is vested in the Secretary of the 
Commission. In any case where the Secretary or his or her designee, in 
his or her discretion, determines that a request for an identifiable 
meeting record should be initially determined by the Commission, the 
Secretary or his or her designee may certify the matter to the 
Commission for decision. In that event, the Commission decision shall be 
made within the time limits set forth in paragraph (b)(5)(iii) of this 
section and shall be final.
    (3) Time limitations on responses to requests. The Secretary or his 
or her designee shall respond to all written requests for copies of 
meeting records within ten (10) working days. The time limitations on 
responses to requests shall begin to run as of the time a request for 
records is received and date stamped by the Office of the Secretary.
    (4) Responses. Form and content. When a requested meeting record has 
been identified and is available for disclosure the requester shall 
either be informed as to where and when the records will be made 
available for inspection or be supplied with a copy. A response denying 
a written request for a meeting record of a closed Commission meeting 
shall be in writing signed by the Secretary and shall include:
    (i) A reference to the specific exemptions under the Government in 
the Sunshine Act (5 U.S.C. 552b(c)) authorizing the denial; and
    (ii) A statement that the denial may be appealed to the Commission 
pursuant to paragraph (b)(5) of this section.
    (5) Appeals to the Commissioners. (i) When the Secretary or his or 
her designee has denied a request for records in whole or in part, the 
requester may, within 30 days of its receipt, appeal the denial to the 
Commissioners of the Consumer Product Safety Commission by writing to 
the attention of the Chairman, Consumer Product Safety Commission, 
Washington, D.C. 20207.
    (ii) The Commission will act upon an appeal within 20 working days 
of its receipt. The time limitations on an appeal begin to run as of the 
time an appeal is received by the Office of the Chairman and date 
stamped.
    (iii) The Commission's action on appeal shall be in writing, signed 
by the Chairman of the Commission if the appeal is denied and shall 
identify the Commissioners who voted for a denial. A denial in whole or 
in part of a request on appeal for records of a closed meeting shall set 
forth the exemption relied on and a brief explanation (without 
disclosing exempt information) of how the exemption applies to the 
records withheld. A denial in whole or in part shall also inform the 
requester of his or her right to seek judicial review as specified in 5 
U.S.C. 552b(h).
    (6) Fees. (i) Fees shall be charged for copies of transcriptions of 
recording or minutes in accordance with the schedule contained in 
paragraph (b)(6)(iii) of this section.
    (ii) There shall be no fee charged for services rendered in 
connection with

[[Page 32]]

production or disclosure of meeting records unless the charges, 
calculated according to the schedule below, exceed the sum of $25.00. 
Where the charges are calculated to be an amount in excess of $25.00, 
the fee charged shall be the difference between $25.00 and the 
calculated charges.
    (iii) The schedule of charges for furnishing copies of meeting 
records is as follows:
    (A) Reproduction, duplication or copying of transcripts or minutes: 
10 cents per page.
    (B) Reproduction of recordings: actual cost basis.
    (C) Transcription (where meeting records are in the form of a 
recording only): actual cost basis.
    (D) Postage: actual cost basis.



PART 1014--POLICIES AND PROCEDURES IMPLEMENTING THE PRIVACY ACT OF 1974--Table of Contents




Sec.
1014.1 Purpose and scope.
1014.2 Definitions.
1014.3 Procedures for requests pertaining to individual records.
1014.4 Requirements for identification of individuals making requests.
1014.5 Disclosure of requested information to individuals.
1014.6 Request for correction or amendment to a record.
1014.7 Agency review of request for correction or amendment of a record.
1014.8 Appeal of initial denial of access, correction or amendment.
1014.9 Disclosure of record to person other than the individual to whom 
          it pertains.
1014.10 Fees.
1014.11 Penalties.
1014.12 Specific exemptions.

    Authority: Privacy Act of 1974 (5 U.S.C. 552a).

    Source: 40 FR 53381, Nov. 18, 1975, unless otherwise noted.



Sec. 1014.1  Purpose and scope.

    This part sets forth the regulations of the Consumer Product Safety 
Commission implementing the Privacy Act of 1974 (Pub. L. 93-579). The 
purpose of these regulations is to inform the public about records 
maintained by the Commission which contain personal information about 
individuals, and to inform those individuals how they may seek access to 
and correct records concerning themselves. These regulations do not 
apply to requests for information made pursuant to the Freedom of 
Information Act (except where such disclosures would constitute an 
invasion of privacy of an individual).



Sec. 1014.2  Definitions.

    As used in this part:
    (a) Individual means a person who is a citizen of the United States 
or an alien lawfully admitted for permanent residence.
    (b) Privacy Act means the Privacy Act of 1974 (Pub. L. 93-579).
    (c) Record means any item of personal information relating to an 
individual, such as educational, employment, financial or medical 
information.
    (d) Statistical record means a record in a system of records 
maintained for statistical research or reporting purposes only and not 
used in whole or in part in making any determination about an 
identifiable individual.
    (e) System of records or records systems means a group of records 
maintained by the Commission from which information may be retrieved by 
the name of an individual or some other individual identifier.
    (f) Maintain includes the collection, use, storage, and 
dissemination of information.



Sec. 1014.3  Procedures for requests pertaining to individual records.

    (a) Any individual may request the Commission to inform him or her 
whether a particular record system named by the individual contains a 
record pertaining to him or her. The request may be made by mail or in 
person during business hours (8:30 a.m. to 5 p.m.) to the Freedom of 
Information/Privacy Act Officer, Office of the Secretary, Consumer 
Product Safety Commission, 4330 East West Highway, Bethesda, Maryland 
(mailing address: Consumer Product Safety Commission, Washington, DC 
20207).
    (b) An individual who believes that the Commission maintains a 
record pertaining to him or her but who cannot determine which record 
system may contain the record, may request assistance by mail or in 
person at the Office of the Secretary during business hours.

[[Page 33]]

    (c) A Commission officer or employee or former employee who desires 
to review or obtain a copy of a personnel record pertaining to him or 
her may make a request by mail or in person at the Office of Human 
Resources Management, Room 523, 4330 East West Highway, Bethesda, 
Maryland (mailing address: Consumer Product Safety Commission, 
Washington, DC 20207).
    (d) Each individual requesting the disclosure of a record or a copy 
of a record shall furnish the following information to the extent known 
with the request to the Freedom of Information/Privacy Act Officer or to 
the Division of Personnel's Processing Unit, as applicable:
    (1) A description of the record sought;
    (2) The approximate date of the record;
    (3) The name or other description of the record system containing 
the record;
    (4) Proof as required in Sec. 1014.4 that he or she is the 
individual to whom the requested record relates; and
    (5) Any other information required by the notice describing the 
record system.
    (e) An individual personally inspecting his or her records may be 
accompanied by other persons of his or her own choosing. The individual 
shall sign a written statement authorizing disclosure of the record in 
the other person's presence.
    (f) Any individual who desires to have a record concerning himself 
or herself disclosed to or mailed to another person may authorize that 
person to act as his or her agent for that specific purpose. The 
authorization shall be in writing, signed by the individual, and shall 
be notarized. An agent requesting the review or copy of another's record 
shall submit with the request the authorization and proof of his or her 
identify as required by Sec. 1014.4(c).
    (g) The parent of any minor individual or the legal guardian of any 
individual who has been declared by a court of competent jurisdiction to 
be incompetent, due to physical or mental incapacity or age, may act on 
behalf of that individual in any matter covered by this part. A parent 
or guardian who desires to act on behalf of such individual shall 
present suitable evidence of parentage or guardianship, by birth 
certificate, certified copy of a court order, or similar documents, and 
proof of the individual's identity in a form that complies with 
Sec. 1014.4(c).
    (h) An individual may request an accounting of all disclosures made 
to other persons or agencies of his or her record, except those 
disclosures made to law enforcement agencies pursuant to section (b)(7) 
of the Privacy Act (5 U.S.C. 552a(b)(7)). A request for accounting, 
whenever made, shall be treated as a request for disclosure of records.

[40 FR 53381, Nov. 18, 1975, as amended at 53 FR 52404, Dec. 28, 1988; 
62 FR 46667, Sept. 4, 1997]



Sec. 1014.4  Requirements for identification of individuals making requests.

    The following proof of identity is required for requests for records 
made pursuant to Sec. 1014.3:
    (a) An individual seeking a record about himself or herself in 
person may establish his or her identity by the presentation of a single 
document bearing a photograph (such as a passport or driver's license) 
or by a presentation of two items of identification which do not bear a 
photograph but do bear both a name and address. An individual who cannot 
provide documentation of his or her identity may provide a written 
statement affirming his or her identity and the fact that he or she 
understands the penalties for making false statements (18 U.S.C. 1001 
and 5 U.S.C. 552a(i)(3)).
    (b) An individual seeking a record by mail shall include a statement 
signed by the individual and properly notarized, that he or she appeared 
before a notary public and submitted proof of identity acceptable to the 
notary public.
    (c) Requests made by an agent, parent, or guardian shall, in 
addition to establishing the identity of the minor or other person he or 
she represents as required by paragraphs (a) and (b), establish his or 
her agency, parentage, or guardianship by documentation.
    (d) In any case in which the Commission determines that the proof of 
identity is not adequate, it may request the

[[Page 34]]

individual to submit additional proof of identity.



Sec. 1014.5  Disclosure of requested information to individuals.

    (a) Upon submission of proof of identity, the Office of the 
Secretary or the Director of Resource Utilization, as applicable, shall 
promptly forward the request to the system manager who will promptly 
allow the individual to see and/or have a copy of the requested record 
or send a copy of the record to the individual by mail, as requested by 
the individual. If the individual asks to see the record, the record 
should be made available for review and/or copying at the location where 
the record is maintained, in the Office of the Secretary, or the 
Director of Resource Utilization, or at the nearest Area Office.
    (b) If the system manager should determine, for any reason, that the 
requested records are exempt from the right of access, a notice of 
denial shall be sent to the requester stating the reasons for denial, 
and the requester's right to appeal the denial in accordance with the 
procedures set forth in Sec. 1014.8 of these regulations.



Sec. 1014.6  Request for correction or amendment to a record.

    (a) Any individual who has reviewed a record pertaining to himself 
or herself may request the Executive Director to correct or amend all or 
any part of the record.
    (b) Each request for a correction or amendment of a record shall be 
in writing and shall contain the following information:
    (1) The name of the individual requesting the correction or 
amendment;
    (2) The name or other description of the system of records in which 
the record sought to be amended is maintained;
    (3) The location of that record in the system of records to the 
extent that it is known;
    (4) A copy of the record sought to be amended or a description of 
that record;
    (5) A statement of the material in the record that should be 
corrected or amended;
    (6) A statement of the specific wording of the correction or 
amendment sought; and
    (7) A statement of the basis for the requested correction or 
amendment including any material that the individual can furnish to 
substantiate the reasons for the amendment sought.

[40 FR 53381, Nov. 18, 1975, as amended at 42 FR 22878, May 5, 1977]



Sec. 1014.7  Agency review of request for correction or amendment of a record.

    (a) Not later than 10 working days after the receipt of the request 
for the correction or amendment of a record under Sec. 1014.6, the 
responsible Commission official shall acknowledge receipt of the request 
and inform the individual whether further information is required before 
the correction or amendment can be considered.
    (b) The responsible Commission official will promptly review the 
request and either make the requested correction or amendment or notify 
the individual of his or her refusal to do so, including in the 
notification the reasons for the refusal, and the appeal procedures 
provided by Sec. 1014.8.
    (c) The responsible Commission official will make each requested 
correction or amendment to a record if that correction or amendment will 
correct anything within the record that is not accurate, relevant, 
timely, or complete. A copy of each corrected or amended record shall be 
furnished to the individual who requested the action. If an accounting 
of disclosure has been kept, all previous recipients of the record shall 
be notified of the correction and its substance.



Sec. 1014.8  Appeal of initial denial of access, correction or amendment.

    (a) Any individual whose request for access, correction or amendment 
to a record is denied, in whole or in part, may appeal that decision 
within 30 working days to the Chairman, Consumer Product Safety 
Commission, Washington, D.C. 20207.
    (b) The appeal shall be in writing and shall:
    (1) Name the individual making the appeal;

[[Page 35]]

    (2) Identify the record to which access is sought or which is sought 
to be corrected or amended;
    (3) Name or describe the record system in which the record is 
contained;
    (4) Contain a short statement describing the correction of amendment 
sought;
    (5) State the name and location of the Commission official who 
initially denied the correction or amendment; and
    (6) State the date of the initial denial.
    (c) Not later than 30 working days after the date on which the 
appeal is received, the Chairman shall complete a review of the appeal 
and make a final decision thereon. However, for good cause shown, the 
Chairman of the Commission may extend the 30-day period. If the Chairman 
so extends the period, he or she shall promptly notify the individual 
requesting the review that the extension has been made.
    (d) If after review of an appeal request, the Chairman also refuses 
to amend the record or grant access to the record in accordance with the 
request, he or she shall send a written notice to the requester 
containing the following information:
    (1) The decision and the reasons for the decision;
    (2) The right of the requester to institute a civil action in a 
Federal District Court for judicial review of the decision; and
    (3) The right of the requester to file with the Chairman a concise 
statement setting forth the reasons for his or her disagreement with the 
denial of the correction or amendment. A copy of the statement of 
disagreement shall be filed with the record in issue, and the record in 
issue shall be so marked as to indicate that there is a disagreement. 
The system manager shall make the statement of disagreement available to 
prior recipients of the disputed record to the extent that an accounting 
of disclosures was maintained, and to any person to whom the record is 
later disclosed, together with a brief statement, if deemed appropriate, 
of the reasons for denying the requested correction or amendment.

[40 FR 53381, Nov. 18, 1975, as amended at 42 FR 22878, May 5, 1977]



Sec. 1014.9  Disclosure of record to person other than the individual to whom it pertains.

    (a) Any person or agency (other than an officer or employee of the 
Commission who has a need for individual records in the performance of 
his or her duty) seeking disclosure of personal records of another 
individual which are contained in a system of records shall submit a 
request in accordance with the Commission's Procedures for Disclosure of 
Production of Information under the Freedom of Information Act (16 CFR 
part 1015, subpart A).
    (b) The determination of whether or not the requested disclosure is 
proper will be made in accordance with the provisions of the Freedom of 
Information Act, as amended (5 U.S.C. 552) and the Commission's policies 
and procedures issued thereunder (16 CFR part 1015).

[41 FR 30324, July 23, 1976]



Sec. 1014.10  Fees.

    The Commission shall not charge an individual for the costs of 
making a search for a record, the costs of reviewing or copying a 
record, or the cost of correcting or amending a record.



Sec. 1014.11  Penalties.

    Any person who makes a false statement in connection with any 
request for a record, or an amendment thereto, under this part, is 
subject to the penalties prescribed in 18 U.S.C. 494, 495, and 1001; and 
5 U.S.C. 552a(i)(3).



Sec. 1014.12  Specific exemptions.

    (a) Injury information. (1) The Bureau of Epidemiology maintains a 
file of Accident Reports (In-Depth Investigations) which are conducted 
on a sample of product related injuries reported to the Commission by 
selected hospital emergency rooms, by consumers through the Commission's 
``Hot-Line'' telephone service and through written consumer complaints 
and by other means such as newspaper reports. The purpose of this record 
system is to compile accident statistics for analyzing the incidence and 
severity of product related injuries.
    (2) Inasmuch as the maintenance of the record system listed in 
paragraph

[[Page 36]]

(a)(1) of this section is authorized by section 5 of the Consumer 
Product Safety Act (15 U.S.C. 2054) and the data are used solely as 
statistical records, the system is exempted from the requirements of the 
Privacy Act relating to making available the accounting of disclosures, 
correction or amendment of the record and the application of these rules 
to the system of records. Specifically, the system is exempt from 5 
U.S.C. 552a(c)(3); (d) (2) and (3); (e)(1); (e)(4) (G), (H) and (I); and 
(f). However, Accident Reports made by Commission employees are 
disclosable in accordance with paragraph (a)(3) of this section.
    (3) Section 25(c) of the Consumer Product Safety Act (15 U.S.C. 
2074(c)) provides that accident or investigation reports made by an 
officer or employee of the Commission shall be made available to the 
public in a manner which will not identify any injured person or any 
person treating him or her, without the consent of the person 
identified. Consequently, an accident or investigation report which 
identifies individuals is available to the injured party or the person 
treating him or her but would not be available for disclosure to a third 
party without the consent of the injured party or person treating him or 
her.
    (4) Since accident or investigation reports are compiled only for 
statistical purposes and are not used in whole or in part in making any 
determination about an individual, they are exempted from the 
requirement to correct or amend a record as provided by subsection 
(d)(2) of the Privacy Act (5 U.S.C. 552a (d)(2)). Exceptions from this 
paragraph, insofar as they relate to amendments or additions, may be 
allowed by the Executive Director.
    (b) Inspector General Investigative Files--CPSC-6. All portions of 
this system of records which fall within 5 U.S.C. 552a(k)(2) 
(investigatory materials compiled for law enforcement purposes) and 5 
U.S.C. 552a(k)(5) (investigatory materials solely compiled for 
suitability determinations) are exempt from 5 U.S.C. 552a(c)(3) 
(mandatory accounting of disclosures); 5 U.S.C. 552a(d) (access by 
individuals to records that pertain to them); 5 U.S.C. 552a(e)(1) 
(requirement to maintain only such information as is relevant and 
necessary to accomplish an authorized agency purpose); 5 U.S.C. 
552a(e)(4)(G) (mandatory procedures to notify individuals of the 
existence of records pertaining to them); 5 U.S.C. 552a(e)(4)(H) 
(mandatory procedures to notify individuals how they can obtain access 
to and contest records pertaining to them); 5 U.S.C. 552a(e)(4)(I) 
(mandatory disclosure of records source categories); and the 
Commission's regulations in 16 CFR part 1014 which implement these 
statutory provisions.
    (c) Enforcement and Litigation Files--CPSC-7. All portions of this 
system of records that fall within 5 U.S.C. 552a(k)(2) (investigatory 
materials compiled for law enforcement purposes) are exempt from 5 
U.S.C. 552a(c)(3) (mandatory accounting of disclosures); 5 U.S.C. 
552a(d) (access by individuals to records that pertain to them); 5 
U.S.C. 552a(e)(1) (requirement to maintain only such information as is 
relevant and necessary to accomplish an authorized agency purpose); 5 
U.S.C. 552a(e)(4)(G) (mandatory procedures to notify individuals of the 
existence of records pertaining to them); 5 U.S.C. 552a(e)(4)(H) 
(mandatory procedures to notify individuals how they can obtain access 
to and contest records pertaining to them); 5 U.S.C. 552a(e)(4)(I) 
(mandatory disclosure of records source categories); and the 
Commission's regulations in 16 CFR part 1014 that implement these 
statutory provisions.

[40 FR 53381, Nov. 18, 1975, as amended at 42 FR 9161, Feb. 15, 1977; 59 
FR 32078, June 22, 1994; 62 FR 48756, Sept. 17, 1997]



PART 1015--PROCEDURES FOR DISCLOSURE OR PRODUCTION OF INFORMATION UNDER THE FREEDOM OF INFORMATION ACT--Table of Contents




        Subpart A--Production or Disclosure Under 5 U.S.C. 552(a)

Sec.
1015.1 Purpose and scope.
1015.2 Public reference facilities.
1015.3 Requests for records and copies.
1015.4 Responses to requests for records; responsibility.

[[Page 37]]

1015.5 Time limitation on responses to requests for records and requests 
          for expedited processing.
1015.6 Responses: Form and content.
1015.7 Appeals from initial denials; reconsideration by the Secretary.
1015.8 Requests received during the course of administrative hearings. 
          [Reserved]
1015.9 Fees for production of records.
1015.10 Commission report of actions to Congress.
1015.11 Disclosure of trade secrets to consultants and contractors; 
          nondisclosure to advisory committees and other government 
          agencies.
1015.12 Disclosure to Congress.

  Subpart B--Exemptions From Production and Disclosure Under 5 U.S.C. 
                                 552(b)

1015.15 Purpose and scope.
1015.16 Exemptions (5 U.S.C. 552(b)).
1015.17 Internal Commission procedure for withholding exempt records.
1015.18 Information submitted to the Commission; request for treatment 
          as exempt material.
1015.19 Decisions on requests for exemption from disclosure under 5 
          U.S.C. 552(b)(4).

 Subpart C--Disclosure of Commission Accident or Investigation Reports 
                         Under 15 U.S.C. 2074(c)

1015.20 Public availability of accident or investigation reports.

    Authority: 15 U.S.C. 2051-2084; 15 U.S.C. 1261-1278; 15 U.S.C. 1471-
1476; 15 U.S.C. 1211-1214; 15 U.S.C. 1191-1204; 5 U.S.C. 552.

    Source: 42 FR 10490, Feb. 22, 1977, unless otherwise noted.



        Subpart A--Production or Disclosure Under 5 U.S.C. 552(a)



Sec. 1015.1  Purpose and scope.

    (a) The regulations of this subpart provide information concerning 
the procedures by which Consumer Product Safety Commission records may 
be made available for inspection and the procedures for obtaining copies 
of records from the Consumer Product Safety Commission. Official records 
of the Consumer Product Safety Commission consist of all documentary 
material maintained by the Commission in any format, including an 
electronic format. These records include those maintained in connection 
with the Commission's responsibilities and functions under the Consumer 
Product Safety Act, as well as those responsibilities and functions 
transferred to the Commission under the Federal Hazardous Substances 
Act, Poison Prevention Packaging Act of 1970, Refrigerator Safety Act, 
and Flammable Fabrics Act, and those maintained under any other 
authorized activity. Official records do not, however, include objects 
or articles such as tangible exhibits, samples, models, equipment, or 
other items of valuable property; books, magazines, or other reference 
material; or documents routinely distributed by the Commission in the 
normal course of business such as copies of Federal Register notices, 
pamphlets, and laws. Official records include only existing records. 
Official records of the Commission made available under the requirements 
of the Freedom of Information Act (5 U.S.C. 552) shall be furnished to 
the public as prescribed by this part 1015. A request by an individual 
for records about himself or herself that are contained in the 
Commission's system of records under the Privacy Act (5 U.S.C. 552a) 
will be processed under the Privacy Act. A request by a third party for 
records that are contained in the Commission's system of records under 
the Privacy Act will be processed administratively under these 
regulations with respect to the time limits and appeals rights 
(Sec. Sec. 1015.5 and 1015.7), but substantively under the applicable 
provisions of first the Freedom of Information Act and then the Privacy 
Act. Documents routinely distributed to the public in the normal course 
of business will continue to be furnished to the public by employees of 
the Commission informally and without compliance with the procedures 
prescribed herein.
    (b) The Commission's policy with respect to requests for records is 
that disclosure is the rule and withholding is the exception. All 
records not exempt from disclosure will be made available. Moreover, 
records which may be exempted from disclosure will be made available as 
a matter of discretion when disclosure is not prohibited by law, or is 
not against the public interest. See, Sec. 1015.15(b). Section 6(a)(2) 
of the Consumer Product Safety Act, 15 U.S.C. 2055(a)(2), prohibits the 
disclosure of trade secrets or other matters referred to in 18 U.S.C. 
1905.

[[Page 38]]

    (c) The Attorney General's Memorandum on the 1974 Amendments to the 
Freedom of Information Act published in February, 1975 is available from 
the Superintendent of Documents and may be consulted in considering 
questions arising under the Freedom of Information Act.

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46196, Sept. 2, 1997]



Sec. 1015.2  Public reference facilities.

    (a) The Consumer Product Safety Commission will maintain in a public 
reference room or area the materials relating to the Consumer Product 
Safety Commission that are required by 5 U.S.C. 552(a)(2) and 552(a)(5) 
to be made available for public inspection and copying. The principal 
location will be in the Office of the Secretary of the Commission. The 
address of this office is:
Office of the Secretary, Consumer Product Safety Commission, Room 502, 
4330 East West Highway, Bethesda, MD 20814.
    (b) This public reference facility will maintain and make available 
for public inspection and copying a current index of the materials 
available at that facility which are required to be indexed by 5 U.S.C. 
552(a)(2). For the purpose of providing the opportunity for greater 
public access to records of the Consumer Product Safety Commission, the 
Commission may establish additional public reference facilities. Each 
such additional reference facility will also maintain and make available 
for public inspection and copying a current index of the materials 
available at that facility which are required to be indexed by 5 U.S.C. 
552(a)(2).
    (c) The Consumer Product Safety Commission will maintain an 
``electronic reading room'' on the World-Wide Web for those records that 
are required by 5 U.S.C. 552(a)(2) to be available by ``computer 
telecommunications.''

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46197, Sept. 2, 1997]



Sec. 1015.3  Requests for records and copies.

    (a) A request for access to records of the Commission shall be in 
writing addressed to the Secretary, Consumer Product Safety Commission, 
Washington, DC 20207. Any written request for records covered by this 
part shall be deemed to be a request for records pursuant to the Freedom 
of Information Act, whether or not the Freedom of Information Act is 
mentioned in the request. An oral request for records will not be 
considered a request for records pursuant to the Freedom of Information 
Act. Responses to oral requests for records shall be made as promptly as 
resources and time restraints permit.
    (b) A request for access to records must reasonably describe the 
records requested. Where possible, specific information regarding dates, 
title, file designations, and other information which may help identify 
the records should be supplied by the requester. If the request relates 
to a matter in pending litigation, where the Commission is a party, the 
court and its location should be identified. Where the information 
supplied by the requester is not sufficient to permit identification and 
location of the records by Commission personnel without an unreasonable 
amount of effort, the requester will be contacted and asked to supply 
the necessary information. Every reasonable effort shall be made by 
Commission personnel to assist in the identification and location of 
requested records.
    (c) If it is determined that a request would unduly burden or 
interfere with the operations of the Commission, the response shall so 
state and shall extend to the requester an opportunity to confer with 
appropriate Commission personnel in an attempt to reduce the request to 
manageable proportions by reformulation and by agreeing on an orderly 
procedure for the production of the records.
    (d) If a requested record cannot be located from the information 
supplied, or is known to have been destroyed or otherwise disposed of, 
the requester shall be so notified by the Secretary or delegate of the 
Secretary.
    (e) The Consumer Product Safety Commission uses a multitrack system 
to process requests under the Freedom of Information Act that is based 
on the amount of work and/or time involved in processing requests. 
Requests for records are processed in the order they are received within 
each track. Upon

[[Page 39]]

receipt of a request for records, the Secretary or delegate of the 
Secretary will determine which track is appropriate for the request. The 
Secretary or delegate of the Secretary may contact requesters whose 
requests do not appear to qualify for the fastest tracks and provide 
such requesters the opportunity to limit their requests so as to qualify 
for a faster track. Requesters who believe that their requests qualify 
for the fastest tracks and who wish to be notified if the Secretary or 
delegate of the Secretary disagrees may so indicate in the request and, 
where appropriate and feasible, will also be given an opportunity to 
limit their requests.

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46197, Sept. 2, 1997]



Sec. 1015.4  Responses to requests for records; responsibility.

    The ultimate responsibility for responding to requests for records 
is vested in the Secretary of the Consumer Product Safety Commission. 
The Secretary or delegate of the Secretary may respond directly or 
forward the request to any other office of the Commission for response. 
In any case where the Secretary or delegate of the Secretary in his/her 
discretion determines that a request for an identifiable record should 
be initially determined by the Commission, the Secretary, or the 
delegate of the Secretary, may certify the matter to the Commission for 
a decision. In that event the Commission decision shall be made within 
the time limits set forth in Sec. 1015.5 and shall be final. The 
Commission response shall be in the form set forth in Sec. 1015.7(d) for 
action on appeal. If no response is made by the Commission within twenty 
working days, or any extension thereof, the requester and the Commission 
may take the action specified in Sec. 1015.7(e).

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46197, Sept. 2, 1997]



Sec. 1015.5  Time limitation on responses to requests for records and requests for expedited processing.

    (a) The Secretary or delegate of the Secretary shall respond to all 
written requests for records within twenty (20) working days (excepting 
Saturdays, Sundays, and legal public holidays). The time limitations on 
responses to requests for records shall begin to run as of the time a 
request for records is received by the Office of the Secretary and a 
date stamp notation placed directly on the request.
    (b) The time for responding to requests for records may be extended 
by the Secretary at the initial stage or by the General Counsel of the 
Commission at the appellate stage up to an additional ten (10) working 
days under the following unusual circumstances:
    (1) The need to search for and collect the requested records from 
field facilities or other establishments that are separate from the 
Office of the Secretary.
    (2) The need to search for, collect and appropriately examine a 
voluminous amount of separate and distinct records which are demanded in 
a single request.
    (3) The need for consultation, which shall be conducted with all 
practicable speed, with another agency having a substantial interest in 
the determination of the request or among two or more components of the 
Commission having substantial subject matter interest therein.
    (c) Any extension of time must be accompanied by written notice to 
the person making the request setting forth the reason(s) for such 
extension and the time within which a response is expected to be made.
    (d) If the Secretary at the initial stage or the General Counsel at 
the appellate stage determines that an extension of time greater than 
ten (10) working days is necessary to respond to a request satisfying 
the ``unusual circumstances'' specified in paragraph (b) of this 
section, the Secretary or the General Counsel shall so notify the 
requester and give the requester the opportunity to:
    (1) Limit the scope of the request so that it may be processed 
within the time limit prescribed in paragraph (b); or
    (2) Arrange with the Secretary or the General Counsel an alternative 
time frame for processing the request or a modified request.
    (e) The Secretary or delegate of the Secretary may aggregate and 
process as a single request requests by the

[[Page 40]]

same requester, or a group of requesters acting in concert, if the 
Secretary or delegate reasonably believes that the requests actually 
constitute a single request which would otherwise satisfy the unusual 
circumstances specified in paragraph (b) of this section, and the 
requests involve clearly related matters.
    (f) The Secretary or delegate of the Secretary will provide 
expedited processing of requests in cases where the requester 
demonstrates a compelling need for such processing.
    (1) The term ``compelling need'' means:
    (i) That a failure to obtain requested records on an expedited basis 
could reasonably be expected to pose an imminent threat to the life or 
physical safety of an individual; or
    (ii) With respect to a request made by a person primarily engaged in 
disseminating information, that there is an urgency to inform the public 
concerning actual or alleged Federal Government activity.
    (2) Requesters for expedited processing must include in their 
requests a statement setting forth the basis for the claim that a 
``compelling need'' exists for the requested information, certified by 
the requester to be true and correct to the best of his or her knowledge 
and belief.
    (3) The Secretary or delegate of the Secretary will determine 
whether to grant a request for expedited processing and will notify the 
requester of such determination within ten (10) days of receipt of the 
request.
    (4) Denials of requests for expedited processing may be appealed to 
the Office of the General Counsel as set forth in Sec. 1015.7 of this 
part. The General Counsel will expeditiously determine any such appeal.
    (5) The Secretary or delegate of the Secretary will process as soon 
as practicable the documents responsive to a request for which expedited 
processing is granted.
    (g) The Secretary may be unable to comply with the time limits set 
forth in this Sec. 1015.5 when disclosure of documents responsive to a 
request under this part is subject to the requirements of section 6(b) 
of the Consumer Product Safety Act, 15 U.S.C. 2055(b), and the 
regulations implementing that section, 16 CFR part 1101. The Secretary 
or delegate of the Secretary will notify requesters whose requests will 
be delayed for this reason.

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46197, Sept. 2, 1997]



Sec. 1015.6  Responses: Form and content.

    (a) When a requested record has been identified and is available for 
disclosure, the requester shall either be supplied with a copy or 
notified as to where and when the record will be made available for 
inspection. If a requester desires to inspect records at one of the 
regional offices of the Commission, the Secretary will ordinarily make 
the records available at the requested regional office. If the payment 
of fees is required the requester shall be advised by the Secretary in 
writing of any applicable fees under Sec. 1015.9 hereof.
    (b) A response denying a written request for a record shall be in 
writing signed by the Secretary or delegate of the Secretary and shall 
include:
    (1) The identity of each person responsible for the denial.
    (2) A reference to the specific exemption or exemptions under the 
Freedom of Information Act authorizing the withholding of the record 
with a brief explanation of how the exemption applies to the record 
withheld; and
    (3) An estimation of the volume of requested material withheld. When 
only a portion or portions of a document are withheld, the amount of 
information deleted shall be indicated on the released portion(s) of the 
record. When technically feasible, the indication of the amount of 
material withheld will appear at the place in the document where any 
deletion is made. Neither an estimation of the volume of requested 
material nor an indication of the amount of information deleted shall be 
included in a response if doing so would harm an interest protected by 
the exemption in 5 U.S.C. 552(b) pursuant to which the material is 
withheld.
    (4) A statement that the denial may be appealed to the Commissioners 
of the Consumer Product Safety Commission. Any such appeal must be made 
within 30 calendar days of receipt of the denial by the requester.

[[Page 41]]

    (c) If no response is made within twenty (20) working days or any 
extension thereof, the requester can consider his or her administrative 
remedies exhausted and seek judicial relief in a United States District 
Court as specified in 5 U.S.C. 552(a)(4)(B). When it appears that no 
response can be made to the requester within the applicable time limit, 
the Secretary or delegate of the Secretary may ask the requester to 
forego judicial relief until a response can be made. The Secretary or 
delegate of the Secretary shall inform the requester of the reason for 
the delay, of the date on which a response may be expected and of his/
her right to seek judicial review as specified in 5 U.S.C. 552(a)(4)(B).

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46197, Sept. 2, 1997]



Sec. 1015.7  Appeals from initial denials; reconsideration by the Secretary.

    (a) When the Secretary or delegate of the Secretary has denied a 
request for records in whole or in part, the requester may, within 30 
days of its receipt, appeal the denial to the General Counsel of the 
Consumer Product Safety Commission, attention of the Secretary, 
Washington, DC 20207.
    (b) The General Counsel, or the Secretary upon reconsideration, will 
act upon an appeal within 20 working days of its receipt. The time 
limitations on an appeal begin to run as of the time an appeal is 
received by the Office of the Secretary and date stamped.
    (c) After reviewing the appeal, the Secretary will reconsider his/
her initial denial. If the Secretary upon reconsideration decides to 
release any or all of the information requested on appeal, an appeal as 
to the information released will be considered moot; and the Secretary 
will so inform the requester and submitter of the information in 
accordance with Sec. Sec. 1015.6(a) and 1015.18(b). If the Secretary 
decides to affirm the initial denial, in whole or in part, the General 
Counsel will decide the appeal within the 20-day time limit or any 
extension thereof in accordance with Sec. 1015.5.
    (d) The General Counsel shall have the authority to grant or deny 
all appeals and, as an exercise of discretion, to disclose records 
exempt from mandatory disclosure under 5 U.S.C. 552(b). In unusual or 
difficult cases the General Counsel may, in his/her discretion, refer an 
appeal to the Commissioners for determination.
    (e) The General Counsel's action on appeal shall be in writing, 
shall be signed by the General Counsel, and shall constitute final 
agency action. A denial in whole or in part of a request on appeal shall 
set forth the exemption relied upon; a brief explanation, consistent 
with the purpose of the exemption, of how the exemption applies to the 
records withheld; and the reasons for asserting it. A denial in whole or 
in part shall also inform the requester of his/her right to seek 
judicial review of the Commission's final determination in a United 
States district court, as specified in 5 U.S.C. 552(a)(4)(B).
    (f) If no response is made to the requester within 20 working days 
or any extension thereof, the requester may consider his/her 
administrative remedies exhausted and seek judicial relief in a United 
States district court. When no response can be made within the 
applicable time limit, the General Counsel shall inform the requester of 
the reason for the delay, of the date by which a response may be 
expected, and of the requester's right to seek judicial review as 
specified in 5 U.S.C. 552(a)(4)(B).
    (g) Copies of all appeals and copies of all actions on appeal shall 
be furnished to and maintained in a public file by the Secretary.

(5 U.S.C. 552(a)(6)(A); 5 U.S.C. 553; 15 U.S.C. 2076(b)(9))

[50 FR 7753, Feb. 26, 1985]



Sec. 1015.8  Requests received during the course of administrative hearings. [Reserved]



Sec. 1015.9  Fees for production of records.

    (a) The Commission will provide, at no charge, certain routine 
information. For other Commission responses to information requests, the 
Secretary shall determine and levy fees for duplication, search, review, 
and other services, in accordance with this section.
    (b) Fees shall be paid by check or money order, payable to the 
Treasury

[[Page 42]]

of the United States and sent to the Commission.
    (c) The following definitions shall apply under this section:
    (1) Direct costs means those expenditures which an agency actually 
incurs in searching for and duplicating (and in the case of commercial 
requesters, reviewing) documents to respond to a FOIA request.
    (2) Search includes all time spent looking for material that is 
responsive to a request, including page-by-page or line-by-line 
identification of material within documents.
    (3) Duplication refers to the process of making a copy of a document 
necessary to respond to a FOIA request.
    (4) Review refers to the process of examining documents located in 
response to a commercial use request to determine whether any portion of 
any document located is permitted to be withheld.
    (5) Commercial use request refers to a request that seeks 
information for a use or purpose that furthers commercial, trade, or 
profit interests.
    (6) Educational institution refers to an entity organized and 
operated exclusively for educational purposes, whose purpose is 
scholarly.
    (7) Non-commercial scientific institution refers to an entity 
organized and operated exclusively for the purpose of conducting 
scientific research, the results of which are not intended to promote 
any particular product or industry.
    (8) Representative of the news media refers to any person or 
organization which regularly publishes or disseminates news to the 
public, in print or electronically.
    (d) A commercial use request may incur charges for duplication, 
search, and review. The following requests may incur charges only for 
duplication: A request from an educational institution for records not 
sought for commercial use; a request from a non-commercial scientific 
institution for records not sought for commercial use; a request from a 
representative of the news media. Any other request may incur charges 
for duplication and search.
    (e) The following fee schedule will apply:
    (1) Copies of documents reproduced on a standard photocopying 
machine: $0.10 per page.
    (2) File searches conducted by clerical personnel: $3.00 for each 
one-quarter hour (a fraction thereof to be counted as one-quarter hour). 
Any special costs of sending records from field locations to 
headquarters for review will be included in search fees, billed at the 
clerical personnel rate.
    (3) File searches conducted by non-clerical or professional or 
managerial personnel: $4.90 for each one-quarter hour (a fraction 
thereof to be counted as one-quarter hour).
    (4) Review of records: $4.90 for each one-quarter hour (a fraction 
thereof to be counted as one-quarter hour).
    (5) Computerized records: $0.10 per page of computer printouts or, 
for central processing, $0.32 per second of central processing unit 
(CPU) time; for printer, $10.00 per 1,000 lines; and for computer 
magnetic tapes or discs, direct costs.
    (6) Postage: Direct-cost basis for mailing requested materials, if 
the requester wants special handling or if the volume or dimensions of 
the materials requires special handling.
    (7) Microfiche: $0.35 for each frame.
    (8) Other charges for materials requiring special reproducing or 
handling, such as photographs, slides, blueprints, video and audio tape 
recordings, or other unusual materials: direct-cost basis.
    (9) Any other service: An appropriate fee established by the 
Secretary, based on direct costs.
    (f) Fees shall be waived as follows:
    (1) No automatic fee waiver shall apply to commercial use requests.
    (2) The first $10.00 of duplication costs shall be waived for 
requests from educational institutions, non-commercial scientific 
institutions, and representatives of the news media.
    (3) For all other requests, the first $10.00 of duplication costs 
and the first $40 of search costs shall be waived.
    (4) The Secretary shall waive or reduce fees whenever disclosure of 
the requested information is in the public interest because it is likely 
to contribute significantly to public understanding of the operations or 
activities of the

[[Page 43]]

government and disclosure of the requested information is not primarily 
in the commercial interest of the requester.
    (5) In making a determination under paragraph (f)(4) of this 
section, the Secretary shall consider the following factors:
    (i) The subject of the request: Whether the subject of the requested 
records concerns the operations or activities of the government.
    (ii) The informative value of the information to be disclosed: 
Whether the disclosure is likely to contribute to an understanding of 
government operations or activities.
    (iii) The contribution to an understanding of the subject by the 
general public likely to result from disclosure: Whether disclosure of 
the requested information will contribute to public understanding.
    (iv) The significance of the contribution to public understanding: 
Whether the disclosure is likely to contribute significantly to public 
understanding of government operations or activities.
    (v) The existence and magnitude of a commercial interest: Whether 
the requester has a commercial interest that would be furthered by the 
requested disclosure; and, if so
    (vi) The primary interest in disclosure: Whether the magnitude of 
the identified commercial interest of the requester is sufficiently 
large, in comparison with the public interest in disclosure, that 
disclosure is primarily in the commercial interest of the requester.
    (6) Any determination made by the Secretary concerning fee waivers 
may be appealed by the requester to the Commission's General Counsel in 
the manner described at Sec. 1015.7.
    (g) Collection of fees shall be in accordance with the following:
    (1) Interest will be charged on amounts billed, starting on the 31st 
day following the day on which the requester received the bill. Interest 
will be at the rate prescribed in 31 U.S.C. 3717.
    (2) Search fees will be imposed (on requesters charged for search 
time) even if no responsive documents are located or if the search leads 
to responsive documents that are withheld under an exemption to the 
Freedom of Information Act. Such fees shall not exceed $25.00, unless 
the requester has authorized a higher amount.
    (3) Before the Commission begins processing a request or discloses 
any information, it will require advance payment if:
    (i) Charges are estimated to exceed $250.00 and the requester has no 
history of payment and cannot provide satisfactory assurance that 
payment will be made; or
    (ii) A requester failed to pay the Commission for a previous Freedom 
of Information Act request within 30 days of the billing date.
    (4) The Commission will aggregate requests, for the purposes of 
billing, whenever it reasonably believes that a requester or group of 
requesters is attempting to separate a request into more than one 
request for the purpose of evading fees.
    (5) If a requester's total bill is less than $9.00, the Commission 
will not request payment.

[52 FR 28979, Aug. 5, 1987, as amended at 62 FR 46198, Sept. 2, 1997]



Sec. 1015.10  Commission report of actions to Congress.

    On or before February 1 of each year, the Commission shall submit a 
report of its activities with regard to freedom of information requests 
during the preceding fiscal year to the Attorney General of the United 
States. This report shall include:
    (a) The number of determinations made by the Commission not to 
comply with requests for records made to the Commission under the 
provisions of this part and the reasons for each such determination.
    (b)(1) The number of appeals made by persons under such provisions, 
the result of such appeals, and the reason for the action upon each 
appeal that results in a denial of information; and
    (2) A complete list of all statutes that the Commission relies upon 
to withhold information under such provisions, a description of whether 
a court has upheld the decision of the Commission to withhold 
information under each such statute, and a concise description of the 
scope of any information withheld.

[[Page 44]]

    (c) The number of requests for records pending before the Commission 
as of September 30 of the preceding year, and the median number of days 
that such requests had been pending before the Commission as of that 
date.
    (d) The number of requests for records received by the Commission 
and the number of requests which the Commission processed.
    (e) The median number of days taken by the Commission to process 
different types of requests.
    (f) The total amount of fees collected by the Commission for 
processing requests.
    (g) The number of full-time staff of the Commission devoted to 
processing requests for records under such provisions, and the total 
amount expended by the Commission for processing such requests.

[42 FR 10490, Feb. 22, 1997, as amended at 62 FR 46198, Sept. 2, 1997]



Sec. 1015.11  Disclosure of trade secrets to consultants and contractors; nondisclosure to advisory committees and other government agencies.

    (a) In accordance with section 6(a)(2) of the CPSA, the Commission 
may disclose information which it has determined to be a trade secret 
under 5 U.S.C. 552(b)(4) to Commission consultants and contractors for 
use only in their work for the Commission. Such persons are subject to 
the same restrictions with respect to disclosure of such information as 
any Commission employee.
    (b) In accordance with section 6(a)(2) of the CPSA, the Commission 
is prohibited from disclosing information which it has determined to be 
a trade secret under 5 U.S.C. 552(b)(4) to advisory committees, except 
when required in the official conduct of their business, or to other 
Federal agencies and state and local governments.



Sec. 1015.12  Disclosure to Congress.

    (a) All records of the Commission shall be disclosed to Congress 
upon a request made by the chairman or ranking minority member of a 
committee or subcommittee of Congress acting pursuant to committee 
business and having jurisdiction over the matter about which information 
is requested.
    (b) An individual member of Congress who requests a record for his 
or her personal use or on behalf of any constituent shall be subject to 
the same rules that apply to members of the general public.

[42 FR 10490, Feb. 22, 1977, as amended at 52 FR 45632, Dec. 1, 1987; 53 
FR 3868, Feb. 10, 1988]



  Subpart B--Exemptions From Production and Disclosure Under 5 U.S.C. 
                                 552(b)



Sec. 1015.15  Purpose and scope.

    (a) The regulations of this subpart provide information concerning 
the types of records which may be withheld from production and 
disclosure by the Consumer Product Safety Commission and the internal 
Commission procedure for withholding exempt records. These regulations 
also provide information on the method whereby persons submitting 
information to the Commission may request that the information be 
considered exempt from disclosure, and information concerning the 
Commission's treatment of documents submitted with a request that they 
be treated as exempt from disclosure.
    (b) No identifiable record requested in accordance with the 
procedures contained in this part shall be withheld from disclosure 
unless it falls within one of the classes of records exempt under 5 
U.S.C 552(b). The Commission will make available, to the extent 
permitted by law, records authorized to be withheld under 5 U.S.C. 
552(b) unless the Commission determines that disclosure is contrary to 
the public interest. In this regard the Commission will not ordinarily 
release documents that provide legal advice to the Commission concerning 
pending or prospective litigation where the release of such documents 
would significantly interfere with the Commission's regulatory or 
enforcement proceedings.
    (c) Draft documents that are agency records are subject to release 
upon request in accordance with this regulation. However, in order to 
avoid any misunderstanding of the preliminary nature of a draft 
document, each draft document released will be marked to

[[Page 45]]

indicate its tentative nature. Similarly, staff briefing packages, which 
have been completed but not yet transmitted to the Commission by the 
Office of the Secretary are subject to release upon request in 
accordance with this regulation. Each briefing package or portion 
thereof released will be marked to indicate that it has not been 
transmitted to or acted upon by the Commission. In addition, briefing 
packages, or portions thereof, which the Secretary upon the advice of 
the Office of the General Counsel has determined would be released upon 
request in accordance with this regulation, will be publicly available 
in the public reference facility established under Sec. 1015.2 promptly 
after the briefing package has been transmitted to the Commissioners by 
the Office of the Secretary. Such packages will be marked to indicate 
that they have not been acted upon by the Commission.
    (d) The exceptions contained in Sec. 1015.16 are as contained in 5 
U.S.C. 552(b). These exemptions will be interpreted in accordance with 
the applicable law at the time a request for production or disclosure is 
considered.

[42 FR 10490, Feb. 22, 1977, as amended at 45 FR 22022, Apr. 3, 1980]



Sec. 1015.16  Exemptions (5 U.S.C. 552(b)).

    (a) Records specifically authorized under criteria established by an 
Executive Order to be kept secret in the interest of national defense or 
foreign policy and are in fact properly classified pursuant to such 
Executive Order.
    (b) Records related solely to the internal personnel rules and 
practices of the Commission.
    (c) Records specifically exempted from disclosure by statute (other 
than section 552b of Title 5, United States Code), provided that such 
statute either requires that the matters be withheld from the public in 
such a manner as to leave no discretion on the issue, or establishes 
particular criteria for withholding or refers to particular types of 
matters to be withheld.
    (d) Trade secrets and commercial or financial information obtained 
from a person and privileged or confidential.
    (e) Interagency or intra-agency memoranda or letters which would not 
be available by law to a party other than an agency in litigation with 
the agency.
    (f) Personnel and medical files and similar files the disclosure of 
which would consititute a clearly unwarranted invasion of personal 
privacy.
    (g) Records or information compiled for law enforcement purposes, 
but only to the extent that the production of such law enforcement 
records or information:
    (1) Could reasonably be expected to interfere with enforcement 
proceedings,
    (2) Would deprive a person of a right to a fair trial or an 
impartial adjudication,
    (3) Could reasonably be expected to constitute an unwarranted 
invasion of personal privacy,
    (4) Could reasonably be expected to disclose the identity of a 
confidential source, including a State, local, or foreign agency or 
authority or any private institution which furnished information on a 
confidential basis, and, in the case of a record or information compiled 
by criminal law enforcement authority in the course of a criminal 
investigation or by an agency conducting a lawful national security 
intelligence investigation, information furnished by a confidential 
source,
    (5) Would disclose techniques and procedures for law enforcement 
investigations or prosecutions, or would disclose guidelines for law 
enforcement investigations or prosecutions if such disclosure could 
reasonably be expected to risk circumvention of the law, or
    (6) Could reasonably be expected to endanger the life or physical 
safety of any individual.
    (h) Records contained in or related to examinations, operating, or 
condition reports prepared by, on behalf of, or for the use of an agency 
responsible for the regulation or supervision of financial institutions.
    (i) Records of geological and geophysical information and data, 
including maps, concerning wells.

[42 FR 10490, Feb. 22, 1977, as amended at 52 FR 44597, Nov. 20, 1987]

[[Page 46]]



Sec. 1015.17  Internal Commission procedure for withholding exempt records.

    Paragraphs (a) and (b) of this section describe the internal 
Commission procedure to be followed for requesting that a record exempt 
from disclosure under the inter- intra-agency memorandum exemption, 5 
U.S.C. 552(b)(5), or the investigatory file exemption, 5 U.S.C. 
552(b)(7), not be disclosed.
    (a) If a bureau or office director believes that it is against the 
public interest to disclose a Commission record prepared by his/her 
bureau or office, he/she may request in writing that the Secretary 
withhold the document. The request must specify why the release would be 
against the public interest.
    (1) If the Secretary agrees to withhold the document, the requester 
shall be notified in writing of the denial and of his/her right to 
appeal in accordance with Sec. 1015.6(b).
    (2) If the Secretary decides to release the document, the bureau or 
office director shall be notified and given two working days within 
which to appeal to the Commissioners. An appeal by a bureau or office 
director shall be in writing addressed to the Chairman. If an appeal is 
taken by a bureau or office director, the Secretary will not disclose 
the document. The Commissioner's action on appeal shall be in accordance 
with Sec. 1015.7(d).
    (b) If a Commissioner believes that it is not in the public interest 
to disclose a Commission record prepared by himself/herself or by his/
her office personnel, the Commissioner shall so inform the Secretary and 
shall specify in writing why the release would be against the public 
interest. The Secretary shall notify the requester in writing of the 
denial in accordance with Sec. 1015.6(b). Any appeal by a requester 
shall be in accordance with Sec. 1015.7 except the provisions for 
reconsideration by the Secretary is not applicable. On appeal, the 
Commissioner who withheld the document shall not participate in the 
decision.

[42 FR 10490, Feb. 22, 1977, as amended at 45 FR 22023, Apr. 3, 1980]



Sec. 1015.18  Information submitted to the Commission; request for treatment as exempt material.

    (a) A person who is submitting information to the Commission, after 
being notified by the Commission of his/her opportunity to request 
confidential treatment for information, must accompany the submission 
with a request that the information be considered exempt from disclosure 
or indicate that a request will be submitted within 10 working days of 
the submission. The failure to make a request within the prescribed time 
limit will be considered an acknowledgment that the submitter does not 
wish to claim exempt status.
    (b) A person who has previously submitted information to the 
Commission, that is now the subject of a Freedom of Information request, 
after being notified by the Commission of his/her opportunity to request 
confidential treatment for the information, must submit a request that 
the information be considered exempt from disclosure within 5 working 
days from receipt of notification. The failure to make a request within 
the prescribed time limit will be considered an acknowledgment that the 
submitter does not wish to claim exempt status.
    (c) Each request for exemption from disclosure under 5 U.S.C. 
552(b)(4) as a trade secret or privileged or confidential commercial or 
financial information must:
    (1) Specifically identify the exact portion(s) of the document 
claimed to be confidential;
    (2) State whether the information claimed to be confidential has 
ever been released in any manner to a person who was not an employee or 
in a confidential relationship with the company;
    (3) State whether the information so specified is commonly known 
within the industry or is readily ascertainable by outside persons with 
a minimum of time and effort;
    (4) State how release of the information so specified would be 
likely to cause substantial harm to the company's competitive position; 
and

[[Page 47]]

    (5) State whether the submitter is authorized to make claims of 
confidentiality on behalf of the person or organization concerned.
    (d) Material received with a request that it be considered exempt 
shall not be maintained in a public file. If, in complying with a 
request for the disclosure of records, it is determined that some or all 
of the material relative to the request has been claimed to be exempt 
from disclosure, the requester will be supplied with a list of this 
material and informed that those portions found not to be exempt will be 
made available as soon as possible.
    (e) No request for exemption from disclosure under 5 U.S.C. 
552(b)(4) should be made by any person who does not intend in good faith 
to assist the Commission in the defense of any judicial proceeding that 
might thereafter be brought to compel the disclosure of information 
which the Commission has determined to be a trade secret or privileged 
or confidential commercial or financial information.



Sec. 1015.19  Decisions on requests for exemption from disclosure under 5 U.S.C. 552(b)(4).

    (a) The Commission generally will not decide whether material 
received with a request for exemption from disclosure under 5 U.S.C. 
552(b)(4) is entitled to be withheld until a request for production or 
disclosure is made for that information. The determination will be based 
on the most authoritative judicial interpretations available at the time 
a request for disclosure or production is considered. Any reasonably 
segregable portion of a record will be disclosed to any person 
requesting such record after deletion of any portions determined to be 
exempt under 5 U.S.C. 552(b)(4). The requester will be given a brief 
description of any information found to be exempt.
    (b) If material received with a request for exemption from 
disclosure under 5 U.S.C. 552(b)(4) is found to be disclosable, in whole 
or in part, the person submitting the material will be notified in 
writing and given 10 calendar days from the receipt of the letter to 
seek judicial relief. In no event, however, will the material be 
returned to the person submitting it.



 Subpart C--Disclosure of Commission Accident or Investigation Reports 
                         Under 15 U.S.C. 2074(c)



Sec. 1015.20  Public availability of accident or investigation reports.

    (a) Accident or investigation reports made by an officer, employee, 
or agent of the Commission are available to the public under the 
procedures set forth in subpart A of this part 1015. No portion of such 
report are subject to the investigatory file exemption contained in the 
Freedom of Information Act (as restated in Sec. 1015.16) except that 
portions identifying any injured person or any person treating such 
injured person will be deleted in accordance with section 25(c)(1) of 
the CPSA. Where disclosure of an accident or investigation report is 
requested by supplying the name of the person injured or other details 
of a specific accident (other than cases where the report is requested 
by the injured person or the injured person's legal representative), the 
Commission will offer to obtain the written consent of the injured party 
or the injured party's representative to the disclosure of the report 
without deleting the party's identity. No deletion of identifying 
portions of such reports or refusal to disclose without the Commission 
having first obtained written consent shall be considered as a denial by 
the Commission of disclosure of Commission records.
    (b) Research reports, demonstration reports, and reports of other 
related activities of the Commission are available to the public under 
the procedures set forth in subpart A of this part 1015.



PART 1016--POLICIES AND PROCEDURES FOR INFORMATION DISCLOSURE AND COMMISSION EMPLOYEE TESTIMONY IN PRIVATE LITIGATION--Table of Contents




Sec.
1016.1 Purpose and policy.
1016.2 Definition.
1016.3 Disclosure and certification of information and records.
1016.4 Testimony of Commission employees in private litigation.


[[Page 48]]


    Authority: 15 U.S.C. 2051-81; 15 U.S.C. 1261-74; 15 U.S.C. 1191-
1204; 15 U.S.C. 1471-76; 15 U.S.C. 1211-14; 5 U.S.C. 552; and 5 U.S.C. 
552a.

    Source: 53 FR 6594, Mar. 2, 1988, unless otherwise noted.



Sec. 1016.1  Purpose and policy.

    (a) The Commission's policy is to make official records available to 
private litigants, to the fullest extent possible.
    (b) The Commission's policy and responsibility is to conserve the 
time of its employees for work on Commission projects and activities. 
Participation of Commission employees in private litigation, in their 
official capacities, is generally contrary to this policy and 
responsibility. In addition, such participation could impair the 
effectiveness of Commission employees as witness in litigation in which 
the Commission is directly involved.



Sec. 1016.2  Definition.

    Private litigation refers to any legal proceeding which does not 
involve the United States government, or any department or agency of the 
U.S. government, as a party.



Sec. 1016.3  Disclosure and certification of information and records.

    (a) Identifiable information and records in the Commission's 
possession will be made available to private litigants in accordance 
with the Commission's Procedures for Disclosure or Production of 
Information under the Freedom of Information Act (16 CFR part 1015), the 
Freedom of Information Act (5 U.S.C. 552), sections 6 and 25(c) of the 
Consumer Product Safety Act (15 U.S.C. 2055 and 2074(c)), and any other 
applicable statutes or regulations.
    (b) The Secretary of the Commission shall certify the authenticity 
of copies of Commission records. Requests must be in writing and must 
include the records to be certified. Requests should be sent to: 
Secretary, Consumer Product Safety Commission, Washington, DC 20207.
    (c) Any subpoena duces tecum served on a Commission employee will be 
handled by the Office of the Secretary in conjunction with the Office of 
the General Counsel. Whenever necessary to prevent the improper 
disclosure of documents, the General Counsel will take steps, in 
conjunction with the Department of Justice, to quash such subpoenas or 
seek protective orders.



Sec. 1016.4  Testimony of Commission employees in private litigation.

    (a) No Commission employee shall testify in his or her official 
capacity in any private litigation, without express authorization from 
the Commission's General Counsel. The Commission may, in its discretion, 
review a decision by the General Counsel to authorize such employee 
testimony. The General Counsel shall in such instances, where time 
permits, advise the Commission, on a no objection basis, of the 
authorization of such employee testimony.
    (b) If any Commission employee is served with a subpoena seeking 
testimony in private litigation, he or she must immediately notify the 
Office of the General Counsel. The Office of the General Counsel, in 
conjunction with the Department of Justice, will (1) take steps to quash 
the subpoena or (2) direct the employee to appear in response to the 
subpoena but refuse to testify on the ground that it is prohibited by 
this section.
    (c) If the General Counsel becomes aware of private litigation in 
which testimony by a Commission employee would be in the interests of 
the Commission, he or she may authorize such testimony, notwithstanding 
paragraph (b) of this section. The Commission may, in its discretion, 
review a decision by the General Counsel to authorize such employee 
testimony. The General Counsel shall in such instances, where time 
permits, advise the Commission, on a no objection basis, of the 
authorization of such employee testimony. Any such testimony must be 
provided in a way that minimizes the use of Commission resources as much 
as possible.

                          PART 1017 [RESERVED]



PART 1018--ADVISORY COMMITTEE MANAGEMENT--Table of Contents




                      Subpart A--General Provisions

Sec.
1018.1 Purpose.

[[Page 49]]

1018.2 Definitions.
1018.3 Policy.
1018.4 Applicability.
1018.5 Advisory Committee Management Officer.

             Subpart B--Establishment of Advisory Committees

1018.11 Charters.
1018.12 Statutory advisory committees.
1018.13 Non-statutory advisory committees.
1018.14 Non-Commission established advisory committees.
1018.15 Membership composition.
1018.16 Membership selection.
1018.17 Appointments.

               Subpart C--Operation of Advisory Committees

1018.21 Calling of meetings.
1018.22 Notice of meetings.
1018.23 Designated Commission employee.
1018.24 Agenda.
1018.25 Minutes and meeting reports.
1018.26 Advisory functions.
1018.27 Public participation.
1018.28 Records and transcripts.
1018.29 Appeals under the Freedom of Information Act.

            Subpart D--Administration of Advisory Committees

1018.31 Support services.
1018.32 Compensation and travel expenses.
1018.33 Change of status.
1018.34 Conflict of interest.
1018.35 Termination of membership.

              Subpart E--Records, Annual Reports and Audits

1018.41 Agency records on advisory committees.
1018.42 Annual report.
1018.43 Comprehensive review.

                   Subpart F--Termination and Renewal

1018.61 Statutory advisory committees.
1018.62 Non-statutory advisory committees.

    Authority: Sec. 8, Pub. L. 92-463, 86 Stat. 770 (5 U.S.C. App. I).

    Source: 41 FR 45882, Oct. 18, 1976, unless otherwise noted.



                      Subpart A--General Provisions



Sec. 1018.1  Purpose.

    This part contains the Consumer Product Safety Commission's 
regulations governing the establishment, operations and administration 
of advisory committees under its jurisdiction. These regulations are 
issued pursuant to section 8(a) of the Federal Advisory Committee Act 
(Pub. L. 92-463, 5 U.S.C. App. I), and supplement Executive Order No. 
11769 (39 FR 7125 (1974)) and Office of Management and Budget Circular 
No. A-63 (Rev.) (39 FR 12369 (1974)).



Sec. 1018.2  Definitions.

    (a) Advisory Committee Act or Act means the Federal Advisory 
Committee Act (Pub. L. 92-463, 5 U.S.C. App. I (1974)).
    (b) OMB Circular No. A-63 means Office of Management and Budget 
Circular No. A-63 (Rev.), entitled ``Advisory Committee Management'' (39 
FR 12369, April 5, 1974), as amended.
    (c) Advisory Committee means any committee, board, commission, 
council, conference, panel, task force or other similar group, or any 
subcommittee or other subgroup, thereof, which is established or used by 
the Commission in the interest of obtaining advice or recommendations 
and which is not composed wholly of full-time officers or employees of 
the Federal Government.
    (d) Statutory advisory committee means an advisory committee 
established or directed to be established by Congress.
    (e) Non-statutory advisory committee means an advisory committee 
established by the Commission, including a committee which was 
authorized, but not established by Congress.
    (f) Ad hoc advisory committee means a non-continuing, non-statutory 
advisory committee established by the Commission for the stated purpose 
of providing advice or recommendations regarding a particular problem 
which must be resolved immediately or within a limited period of time.
    (g) Non-Commission established advisory committee means an advisory 
committee established by a Federal, State, or local instrumentality 
other than the Commission, or by a private organization or group and 
utilized by the Commission for advisory services.
    (h) GSA Secretariat means the Committee Management Secretariat of 
the General Services Administration.

[[Page 50]]

    (i) Chairman means the Chairman of the Consumer Product Safety 
Commission.

[41 FR 45882, Oct. 18, 1976, as amended at 46 FR 63248, Dec. 31, 1981]



Sec. 1018.3  Policy.

    In application of this part, Commission officials shall be guided by 
the Advisory Committee Act, the statutes creating the Commission's 
advisory committees, and by the directives in Executive Order No. 11769 
and OMB Circular No. A-63. Principles to be followed include:
    (a) Limiting the number of advisory committees to those that are 
essential and terminating any committee not fulfilling its purpose;
    (b) Insuring effective use of advisory committees and their 
recommendations, while assuring that decisional authority is retained by 
the responsible Commission officers;
    (c) Providing clear goals, standards, and uniform procedures with 
respect to the establishment, operation, and administration of advisory 
committees;
    (d) Ensuring that adequate information is provided to the public 
regarding advisory committees; and
    (e) Ensuring adequate opportunities for access by the public to 
advisory committee meetings and information.



Sec. 1018.4  Applicability.

    (a) This part shall apply to all advisory committees (whether 
statutory or non-statutory) subject to the jurisdiction of the 
Commission. This part also shall apply to ad hoc advisory committees and 
non-Commission established advisory committees when they are performing 
advisory services for the Commission.
    (b) Nothing in this part shall apply to any of the following types 
of organizations:
    (1) Any local civic group whose primary function is that of 
rendering a public service with respect to a Federal program;
    (2) Any state or local government committee, council, board, 
commission, or similar group established to advise or make 
recommendations to State or local officials or agencies;
    (3) Any committee whether advisory, interagency, or intraagency 
which is composed wholly of full-time officers or employees of the 
Federal Government;
    (4) Persons or organizations having contractual relationships with 
the Commission; and
    (5) Persons or organizations developing consumer product safety 
standards under section 7 of the Consumer Product Safety Act (15 U.S.C. 
2056).
    (c) This part shall not apply to a committee or other group to the 
extent that it is specifically exempted by statute from the Federal 
Advisory Committee Act.

[41 FR 45882, Oct. 18, 1976, as amended at 46 FR 63248, Dec. 31, 1981]



Sec. 1018.5  Advisory Committee Management Officer.

    The Chairman shall designate an Advisory Committee Management 
Officer who shall:
    (a) Exercise control and supervision over the establishment, 
procedures, and accomplishments of all advisory committees established 
or utilized by the Commission;
    (b) Assemble and maintain the reports, records, and other papers of 
any such committee during its existence, and carry out, on behalf of the 
Secretary of the Commission, the provisions of section 552 of Title 5, 
United States Code (Freedom of Information Act) and the Commission's 
Procedures for Disclosure or Production of Information Under the Freedom 
of Information Act (16 CFR part 1015) with respect to such reports, 
records, and other papers; and
    (c) Perform such other functions as specified in this part.



             Subpart B--Establishment of Advisory Committees



Sec. 1018.11  Charters.

    (a) No advisory committee shall meet or take any action until its 
charter has been filed with the GSA Secretariat in accordance with the 
requirements of section 9(c) of the Federal Advisory Committee Act.
    (b) The Advisory Committee Management officer shall have 
responsibility

[[Page 51]]

for the preparation and filing of charters.

[41 FR 45882, Oct. 18, 1976, as amended at 46 FR 63249, Dec. 31, 1981]



Sec. 1018.12  Statutory advisory committees.

    The Commission has one statutory advisory committee subject to the 
Federal Advisory Committee Act. The Toxicological Advisory Board was 
established by the Commission on December 22, 1978, pursuant to section 
20 of the Federal Hazardous Substances Act, as amended (Pub. L. 95-631, 
92 Stat. 3747, 15 U.S.C. 1275).

[46 FR 63248, Dec. 31, 1981]



Sec. 1018.13  Non-statutory advisory committees.

    (a) In proposing to establish a non-statutory advisory committee, 
the Commission shall follow the procedural requirements of section 
9(a)(2) of the Advisory Committee Act and section 6(a) of OMB Circular 
No. A-63.
    (b) A non-statutory advisory committee shall not be established if 
the proposed function can be performed effectively by Commission 
personnel, by an existing advisory committee, or by another Federal 
agency.



Sec. 1018.14  Non-Commission established advisory committees.

    (a) To the extent practicable, the Commission shall utilize advisory 
committees already established by Federal, State, or local government or 
by private organizations, rather than establish a new advisory committee 
or expand the functions of an existing Commission advisory committee.
    (b) In utilizing a non-Commission established advisory committee, 
Commission officials shall follow the applicable provisions of this part 
and the requirements of the Advisory Committee Act.



Sec. 1018.15  Membership composition.

    The Toxicological Advisory Board, as specified in section 20 of the 
Federal Hazardous Substances Act, as amended (Pub. L. 95-631, 92 Stat. 
3747, 15 U.S.C. 1275), shall be composed of nine members appointed by 
the Commission. Each member of the Board shall be qualified by training 
and experience in one or more fields applicable to the duties of the 
Board, and at least three of the members of the Board shall be members 
of the American Board of Medical Toxicology. The Commission will seek a 
balanced membership, including individuals representative of consumers, 
government and industry.

[46 FR 63248, Dec. 31, 1981]



Sec. 1018.16  Membership selection.

    (a) Whenever new applicants are required for a Commission advisory 
committee, public notice will be issued in the Federal Register inviting 
individuals to submit, on or before a specified date, applications or 
nominations for membership.
    (b) An applicant for membership on an advisory committee shall 
disclose all affiliations, either paid or as a volunteer, that bear any 
relationship to the subject area of product safety or to membership on 
the advisory committee. This disclosure shall include both current 
affiliations and relevant past affiliations.
    (c) The Secretary of the Commission shall, from time to time, 
appoint a Candidate Evaluation Panel consisting of qualified, staff 
members of the Commission, including the Advisory Committee Management 
Officer.
    (d) The Candidate Evaluation Panel, using selection criteria 
established by the Commission, shall evaluate all candidates and submit 
to the Commissioners the names of those candidates it recommends for 
membership. Where possible, at least three candidates shall be 
recommended for each appointment to be made. Final selection for 
membership shall be made by the Commissioners.
    (e) The membership of each Commission Advisory Committee shall be 
fairly balanced in terms of geographic location, age, sex, and race.



Sec. 1018.17  Appointments.

    (a) The Chairman shall appoint as members to advisory committees 
those persons selected by the Commissioners.
    (b) The term of appointment to an advisory committee shall be for 
two years, unless otherwise specified by the Commission. To promote 
maximum participation, an advisory committee

[[Page 52]]

member may serve for only one consecutive full term. This subsection 
shall not be deemed to affect the term of appointment of any present 
member of an advisory committee in effect on the original effective date 
of this part, September 24, 1975.
    (c) A vacancy that occurs during the term of an appointment normally 
will be filled by the Commission from the applications or nominations on 
file. Appointment to any such vacancy will be for the unexpired portion 
of the original appointment. Appointees to such an unexpired term may be 
reappointed for a full two-year term.
    (d) Notwithstanding paragraphs (b) and (c) above, members of the 
Toxicological Advisory Board shall be appointed for terms of three 
years. Members may be reappointed for a subsequent three-year term. Any 
vacancy on the Board shall be filled in the same manner in which the 
original appointment was made. Any person appointed to fill a vacancy 
occurring before the expiration of the term for which his or her 
predecessor was appointed shall serve only for the remainder of such 
term.

[41 FR 45882, Oct. 18, 1976, as amended at 43 FR 60876, Dec. 29, 1978]



               Subpart C--Operation of Advisory Committees



Sec. 1018.21  Calling of meetings.

    Advisory committees shall, as a general rule, meet four times per 
year, except that, as provided by statute, the Toxicological Advisory 
Board shall meet not less than two times each year. No advisory 
committee shall hold a meeting without advance approval of the Chairman 
or the Commission official designated under Sec. 1018.23(a). Before 
giving such advance approval, the Chairman or Commission official shall 
notify the Commission of the date of the proposed meeting.

[41 FR 45822, Oct. 18, 1976, as amended at 43 FR 60876, Dec. 29, 1978]



Sec. 1018.22  Notice of meetings.

    (a) Meetings shall be called by written and/or oral notice to all 
members of the advisory committee.
    (b) Notice of each advisory committee meeting shall be published in 
the Federal Register as well as other means to give widespread public 
notice, at least 15 calendar days before the date of the meeting, except 
that shorter notice may be provided in emergency situations. Reasons for 
such emergency exceptions shall be made part of the meeting notice.
    (c) A meeting notice shall include:
    (1) The official designation of the committee;
    (2) The address and site of the meeting;
    (3) The time of the meeting;
    (4) The purpose of the meeting, including where appropriate, a 
summary of the agenda;
    (5) Whether, or the extent to which, the public will be permitted to 
attend or participate;
    (6) An explanation of how any person who wishes to do so may file a 
written statement with the committee before, during, or after the 
meeting; and
    (7) The procedure by which a public attendee may present an oral 
statement or question to members of the committee.



Sec. 1018.23  Designated Commission employee.

    (a) The Chairman shall designate a member of the Commission or other 
Commission officer or employee to chair or attend each meeting of each 
advisory committee.
    (b) Unless otherwise provided in the statute creating a statutory 
advisory committee, the committee normally will be chaired, on a 
rotating basis, by a member of the Commission.
    (c) No advisory committee shall conduct any meeting in the absence 
of the officer or employee designated under paragraph (a) of this 
section.
    (d) The officer or employee designated under paragraph (a) of this 
section is authorized to adjourn any advisory committee meeting whenever 
he or she determines adjournment to be in the public interest.



Sec. 1018.24  Agenda.

    Prior to each advisory committee meeting, the Advisory Committee 
Management Officer shall prepare and,

[[Page 53]]

after approval by the officer or employee designated under Sec. 1018.23 
(a), shall distribute to each committee member the agenda for that 
meeting. The agenda for a meeting shall list the matters to be discussed 
at the meeting and shall indicate whether and when any part of the 
meeting will concern matters which are exempt from public disclosure 
under the Freedom of Information Act (5 U.S.C. 552(b) or section 6(a)(2) 
of the Consumer Product Safety Act (15 U.S.C. 2045(a)(2)).



Sec. 1018.25  Minutes and meeting reports.

    (a) The Advisory Committee Management Officer shall be responsible 
for the preparation of detailed minutes of each meeting of each advisory 
committee. The minutes shall include at least the following:
    (1) The time and place of the meeting;
    (2) A list of advisory committee members and staff and Commission 
employees present at the meeting;
    (3) A complete summary of all matters discussed and conclusions 
reached;
    (4) Copies of all reports received, issued, or approved by the 
advisory committee; and
    (5) A description of public participation, including a list of 
members of the public who presented oral or written statements and an 
estimate of the number of members of the public who attended the 
meeting.
    (b) The chairman of the advisory committee shall certify the 
accuracy of the minutes.
    (c) Whenever a non-Commission established committee convenes and, at 
the request of the Commission, a portion of the session is allocated to 
the rendering of advisory services to the Commission, the Advisory 
Committee Management Officer shall attend and prepare minutes for that 
portion of the meeting in accordance with this section.
    (d) In addition to the information required by subsection (a) of 
this section, the minutes of the Toxicological Advisory Board shall 
specify the reasons for all conclusions reached and, where conclusions 
are not unanimous, the Board is encouraged to submit minority or 
dissenting opinions.

[41 FR 45882, Oct. 18, 1976, as amended at 43 FR 60876, Dec. 29, 1978]



Sec. 1018.26  Advisory functions.

    (a) Unless otherwise specifically provided by statute, advisory 
committees shall be utilized solely for advisory functions.
    (b) The Commission shall ensure that the advice and recommendations 
of advisory committees shall not be in-appropriately influenced by the 
Commission, its staff, or by any special interest, but will be the 
result of the advisory committee's independent judgment.



Sec. 1018.27  Public participation.

    (a) The Commission is committed to a policy of encouraging public 
participation in its activities and will hold all advisory committee 
meetings open to the public.
    (b) The guidelines in section 8(c) of OMB Circular A-63 shall be 
followed in providing public access to advisory committee meetings.



Sec. 1018.28  Records and transcripts.

    (a) Subject to section 552 of title 5, United States Code (Freedom 
of Information Act) and 16 CFR part 1015 (Commission's Procedures for 
Disclosure or Production of Information under the Freedom of Information 
Act), the records, reports, transcripts, minutes, appendices, working 
papers, drafts, studies, agendas or other documents which were made 
available to or prepared for or by an advisory committee shall be made 
available for public inspection and copying in the Commission's Office 
of the Secretary.
    (b) Advisory Committee documents shall be made available until the 
advisory committee ceases to exist. Disposition of the advisory 
committee documents shall be determined by the Secretary of the 
Commission at that time.



Sec. 1018.29  Appeals under the Freedom of Information Act.

    Appeals from the denial of access to advisory committee documents 
shall be considered in accordance with the

[[Page 54]]

Commission's Procedures for Disclosure or Production of Information 
under the Freedom of Information Act (16 CFR part 1015).



            Subpart D--Administration of Advisory Committees



Sec. 1018.31  Support services.

    Unless the statutory authority for a particular advisory committee 
provides otherwise, the Advisory Committee Management Officer shall be 
responsible for providing and overseeing all necessary support services 
for each advisory committee established by or reporting to the 
Commission. Support services include providing committee staff, meeting 
rooms, supplies, and funds, including funds for the publication of 
reports.



Sec. 1018.32  Compensation and travel expenses.

    (a) A single rate of compensation will be offered to members of all 
advisory committees with the exception of government employees and those 
individuals whose company or organization prohibits such payment. This 
rate shall be $100 per day for each day in attendance at the meeting and 
for each day of travel.
    (b) The Commission shall determine per diem and travel expenses for 
members, staffs, and consultants in accordance with section 7(d) of the 
Advisory Committee Act and section 11 of OMB Circular No. A-63.
    (c) Members of advisory committees, while engaged in the performance 
of their duties away from their homes or regular place of business, may 
be allowed travel expenses including per diem in lieu of expenses as 
authorized by 5 U.S.C. 5703.



Sec. 1018.33  Change of status.

    Any advisory committee member who changes his or her affiliation or 
who assumes an additional affiliation, so as to actually or potentially 
affect his or her representational capacity on an advisory committee 
(upon which the member's application was based), shall immediately 
notify, in writing, the Advisory Committee Management Officer. Such 
notification shall include all relevant information concerning the 
change in affiliation and a statement by the member expressing his or 
her opinion regarding the implications of such change. The notification 
and any other relevant information shall be evaluated by the 
Commissioners to determine the appropriateness of the member's continued 
membership on the advisory committee.



Sec. 1018.34  Conflict of interest.

    Members of the Commission's statutory advisory committees are not 
legally subject to the standards of conduct and conflict of interest 
statutes and regulations applicable to Commission employees. However, it 
is important to avoid situations in which a member of an advisory 
committee has an actual or apparent conflict of interest between the 
member's private interests (or the interests of the member's 
organization) and the member's interest in properly performing his or 
her duties as an advisory committee member. To preclude any such actual 
or apparent conflict of interest, committee members shall be subject to 
the following guidelines:
    (a) Committee members should not personally participate, either for 
themselves or on behalf of an organization, in negotiations, or the 
preparation of negotiations, for contracts with or grants from the 
Commission. Nor should committee members, either as an individual or on 
behalf of an organization, become personally involved in the performance 
of work under such a negotiated contract or grant awarded by the 
Commission. Committee members may participate in preparing bids for and 
performing work under advertised contracts where price is the single 
factor in the determination of award.
    (b) Committee members should not become personally involved in the 
preparation or submission of a proposal to develop a safety standard or 
regulation under any of the Acts administered by the Commission.
    (c) Committee members representing anyone in a professional capacity 
in a proceeding before the Commission should, pursuant to paragraph (e) 
and (f) of this section, advise the committee chairperson and the other 
members of the committee on which he or

[[Page 55]]

she serves of the representation prior to the committee's discussion 
regarding that proceeding. Where the chairperson of the committee 
determines that the representation involves a conflict or the appearance 
of a conflict of interest, the member will be asked to withdraw from the 
discussion of the proceeding. In circumstances where withdrawal from the 
committee's discussion or consideration of the matter is determined by 
the Commission to be insufficient to avoid a conflict or apparent 
conflict of interest, continued representation may be considered 
incompatible with membership on the committee.
    (d) Committee members should exercise caution to ensure that their 
public statements are not interpreted to be official policy statements 
of the Commission.
    (e) Committee members shall disclose to the committee chairperson 
and to the other members of the committee on which he or she serves, any 
special interest in a particular proceeding or matter then pending 
before the committee which in any way may affect that member's position, 
views or arguments on the particular proceeding or matter. The 
disclosure shall be made orally prior to the commencement of the 
discussion. ``Special interest'' is not intended to include a member's 
general interest in presenting a position, views, or arguments in his or 
her representational capacity.
    (f) Where the chairperson of the committee determines that the 
disclosure referred to in paragraph (e) of this section reveals a 
conflict or apparent conflict of interest with respect to a member's 
involvement in the committee's consideration or discussion of a 
particular matter, the member will be asked to withdraw from the 
discussion of the matter.
    (g) The provisions of paragraphs (a) and (b) of this section do not 
apply to state and local government officers and employees.



Sec. 1018.35  Termination of membership.

    Advisory committee membership may be terminated at any time upon a 
determination by the Commission that such action is appropriate.



              Subpart E--Records, Annual Reports and Audits



Sec. 1018.41  Agency records on advisory committees.

    (a) In accordance with section 12(a) of the Advisory Committee Act, 
the Advisory Committee Management Officer shall maintain, in the Office 
of the Secretary, records which will fully disclose the nature and 
extent of the activities of each advisory committee established or 
utilized by the Commission.
    (b) The records shall include a current financial report itemizing 
expenditures and disclosing all funds available for each advisory 
committee during the current fiscal year.
    (c) The records shall also include a complete set of the charters of 
the Commission's advisory committee and copies of the annual reports on 
advisory committees.



Sec. 1018.42  Annual report.

    (a) The Advisory Committee Management Officer shall prepare an 
annual report on the Commission's advisory committees for inclusion in 
the President's annual report to Congress as required by section 6(c) of 
the Advisory Committee Act. This report shall be prepared and submitted 
in accordance with General Services Administration guidelines (39 FR 
44814, December 27, 1974).
    (b) Results of the annual comprehensive review of advisory committee 
made under Sec. 1018.43 shall be included in the annual report.



Sec. 1018.43  Comprehensive review.

    A comprehensive review of all Commission established or utilized 
advisory committees shall be made annually in accordance with section 10 
of the GSA Circular No. A-63, as amended, and shall be submitted to the 
GSA Secretariat by November 30 of each year.

[41 FR 45882, Oct. 18, 1976, as amended at 46 FR 63249, Dec. 31, 1981]

[[Page 56]]



                   Subpart F--Termination and Renewal



Sec. 1018.61  Statutory advisory committees.

    A new charter shall be filed for each statutory advisory committee 
in accordance with section 9(c) of the Advisory Committee Act and 
Sec. 1018.11 upon the expiration of each successive two-year period 
following the date of enactment of the statute establishing or requiring 
the establishment of the committee.



Sec. 1018.62  Non-statutory advisory committees.

    (a) Each non-statutory advisory committee established by the 
Commission after the effective date of this part shall terminate not 
later than two years after its establishment unless prior to that time 
it is renewed in accordance with paragraph (c) of this section.
    (b) Each non-statutory advisory committee which is renewed by the 
Commission shall terminate not later than two years after its renewal 
unless prior to that time it is again renewed in accordance with 
paragraph (c) of this section.
    (c) Before a non-statutory advisory committee can be renewed by the 
Commission, the chairman shall inform the GSA Secretariat by letter not 
more than 60 days nor less than 30 days before the committee expires of 
the following:
    (1) His or her determination that renewal is necessary and is in the 
public interest;
    (2) The reasons for his or her determination;
    (3) The Commission's plan to attain balanced membership of the 
committee, and;
    (4) An explanation of why the committee's functions cannot be 
performed by the Commission or by another existing advisory committee.
    (d) If the GSA Secretariat concurs, the Chairman shall certify in 
writing that the renewal of the advisory committee is in the public 
interest and shall publish notice of the renewal in the Federal Register 
and shall file a new charter.

[41 FR 45882, Oct. 18, 1976, as amended at 46 FR 63249, Dec. 31, 1981]



PART 1019--EXPORT OF NONCOMPLYING, MISBRANDED, OR BANNED PRODUCTS--Table of Contents




Subpart A--Procedures for Export of Noncomplying, Misbranded, or Banned 
                                Products

Sec.
1019.1 Purpose, applicability, and exemptions.
1019.2 Definitions.
1019.3 General requirements for notifying the Commission.
1019.4 Procedures for notifying the Commission; content of the 
          notification.
1019.5 Time notification must be made to Commission; reductions of time.
1019.6 Changes to notification.
1019.7 Commission notification of foreign governments.
1019.8 Confidentiality.

 Subpart B--Statement of Policy and Interpretation Concerning Export of 
              Noncomplying, Misbranded, or Banned Products

1019.31 Purpose and scope.
1019.32 Statutory provisions.
1019.33 Statement of policy and interpretation.

    Authority: 15 U.S.C. 1196, 1202, 1263, 1264, 1273, 2067, 2068.

    Source: 61 FR 29647, June 12, 1996, unless otherwise noted.



Subpart A--Procedures for Export of Noncomplying, Misbranded, or Banned 
                                Products



Sec. 1019.1  Purpose, applicability, and exemptions.

    (a) Purpose. The regulations in this subpart A of this part 1019 
establish the procedures exporters must use to notify the Consumer 
Product Safety Commission of their intent to export from the United 
States products which are banned or fail to comply with an applicable 
safety standard, regulation, or statute. These regulations also set 
forth the procedures the Commission uses in transmitting the 
notification of export of noncomplying products to the country to which 
those products will be sent. The Consumer Product Safety

[[Page 57]]

Act Authorization Act of 1978 (Pub. L. 95-631), which became effective 
November 10, 1978, established these notification requirements and 
authorizes the Commission to issue regulations to implement them.
    (b) Applicability. These regulations apply to any person or firm 
which exports from the United States and item which is:
    (1) A consumer product that does not conform to an applicable 
consumer product safety rule issued under sections 7 and 9 of the 
Consumer Product Safety Act (15 U.S.C. 2056, 2058), or which has been 
declared to be a banned hazardous product under provisions of sections 8 
and 9 of that Act (15 U.S.C. 2057, 2058); or
    (2) A misbranded hazardous substance or a banned hazardous substance 
within the meaning of sections 2(p) and 2(q) of the Federal Hazardous 
Substances Act (15 U.S.C. 1261); or
    (3) A fabric or related material or an item of wearing apparel or 
interior furnishing made of fabric or related material which fails to 
conform with an applicable flammability standard or regulations issued 
under section 4 of the Flammable Fabrics Act (15 U.S.C. 1191, 1193).
    (c) Exemption for certain items with noncomplying labeling. The 
exporter of an item that fails to comply with a standard or regulation 
only because it is labeled in a language other than English need not 
notify the Commission prior to export if the product is labeled with the 
required information in the language of the country to which the product 
will be sent.
    (d) Exemption for samples. The exporter of an item that fails to 
comply with a standard or regulation, but which is intended for use only 
as a sample and not for resale, need not notify the Commission prior to 
export, if the item is conspicuously and labeled in English with the 
statement: ``Sample only. Not for resale.'' (The Commission encourages 
exporters to provide this label, in addition, in the language of the 
importing country, but does not require the foreign language labeling.) 
To qualify as a sample shipment under this exemption, the quantity of 
goods involved must be consistent with prevalent trade practices with 
respect to the specific product.
    (e) Exemption for items not in child-resistant packaging. The 
exporter of an item which is a ``misbranded hazardous substance'' within 
the meaning of section 2(p) of the Federal Hazardous Substances Act (15 
U.S.C. 1261(p)) only because it fails to comply with an applicable 
requirement for child-resistant packaging under the Poison Prevention 
Packaging Act of 1970 (15 U.S.C. 1471 et seq.) need not notify the 
Commission prior to export.



Sec. 1019.2  Definitions.

    As used in this subpart A of this part 1019:
    (a) Consignee means the person, partnership, corporation or entity 
in a foreign country to whom noncomplying goods are sent;
    (b) Export means to send goods outside the United States or United 
States possessions for purposes of trade, except the term does not apply 
to sending goods to United States installations located outside the 
United States or its possessions;
    (c) Exporter means the person, partnership, corporation or entity 
that initiates the export of noncomplying goods;
    (d) Noncomplying goods means any item described in Sec. 1019.1(b), 
except for those items excluded from the requirements of these 
regulations by Sec. 1019.1 (c), (d), and (e).



Sec. 1019.3  General requirements for notifying the Commission.

    Not less than 30 days before exporting any noncomplying goods 
described in Sec. 1019.1(b), the exporter must file a statement with the 
Consumer Product Safety Commission, as described in Sec. Sec. 1019.4 and 
1019.5 of this subpart A. The exporter need not notify the Commission 
about the export of items described in Sec. 1019.1 (c), (d), or (e). As 
described in Sec. 1019.5, the exporter may request the Commission to 
allow the statement to be filed between 10 and 29 days before the 
intended export, and the request may be granted for good cause.

[[Page 58]]



Sec. 1019.4  Procedures for notifying the Commission; content of the notification.

    (a) Where notification must be filed. The notification of intent to 
export shall be addressed to the Assistant Executive Director for 
Compliance, Consumer Product Safety Commission, Washington, DC 20207.
    (b) Coverage of notification. An exporter must file a separate 
notification for each country to which noncomplying goods are to be 
exported. Each notification may include a variety of noncomplying goods 
being shipped to one country. The notification may include goods 
intended to be shipped to one country in any one year, unless the 
Assistant Executive Director of Compliance directs otherwise in writing.
    (c) Form of notification. The notification of intent to export must 
be in writing and must be entitled: ``Notification of Intent to Export 
Noncomplying Goods to [indicate name of country].'' The Commission has 
no notification forms, but encourages exporters to provide the required 
information in the order listed in paragraphs (d) and (e) of this 
section.
    (d) Content of notification; required information. The notification 
of intent to export shall contain the information required by this 
subsection. If the notification covers a variety of noncomplying goods 
the exporter intends to export to one country, the information required 
below must be clearly provided for each class of goods, and may include 
an estimate of the information required in paragraphs (d) (3) and (5) of 
this section. The required information is:
    (1) Name, address and telephone number of the exporter;
    (2) Name and address of each consignee;
    (3) Quantity and description of the goods to be exported to each 
consignee, including brand or trade names or model or other identifying 
numbers;
    (4) Identification of the standards, bans, regulations and statutory 
provisions applicable to the goods being exported, and an accurate 
description of the manner in which the goods fail to comply with 
applicable requirements; and
    (5) Anticipated date of shipment and port of destination.
    (e) Optional information. In addition to the information required by 
paragraph (d) of this section, the notification of intent to export may 
contain, at the exporter's option, the following information:
    (1) Copies of any correspondence from the government of the country 
of destination of the goods indicating whether the noncomplying goods 
may be imported into that country; and
    (2) Any other safety-related information that the exporter believes 
is relevant or useful to the Commission or to the government of the 
country of intended destination.
    (f) Signature. The notification of intent to export shall be signed 
by the owner of the exporting firm if the exporter is a sole-
proprietorship, by a partner if the exporter is a partnership, or by a 
corporate officer if the exporter is a corporation.



Sec. 1019.5  Time notification must be made to Commission; reductions of time.

    (a) Time of notification. The notification of intent to export must 
be received by the Commission's Assistant Executive Director for 
Compliance at least 30 days before the noncomplying goods are to leave 
the customs territory of the United States. If the notification of 
intent to export includes more than one shipment of noncomplying goods 
to a foreign country, the Assistant Executive Director for Compliance 
must receive the notification at least 30 days before the first shipment 
of noncomplying goods is to leave the customs territory of the United 
States.
    (b) Incomplete notification. Promptly after receiving notification 
of intent to export, the Assistant Executive Director will inform the 
exporter if the notification of intent to export is incomplete and will 
described which requirements of Sec. 1019.4 are not satisfied. The 
Assistant Executive Director may inform the exporter that the 30-day 
advance notification period will not begin until the Assistant Executive 
Director receives all the required information.
    (c) Requests for reduction in 30-day notification requirement. Any 
exporter may

[[Page 59]]

request an exemption from the requirement of 30-day advance notification 
of intent to export by filing with the Commission's Assistant Executive 
Director for Compliance (Washington, DC 20207) a written request that 
the time be reduced to a time between 10 and 30 days before the intended 
export. The request for reduction in time must be received by the 
Assistant Executive Director for Compliance at least 3 working days 
before the exporter wishes the reduced time period to begin. The request 
must:
    (1) Be in writing;
    (2) Be entitled ``Request for Reduction of Time to File Notification 
of Intent to Export Noncomplying Goods to [indicate name of country]'';
    (3) Contain a specific request for the time reduction requested to a 
time between 10 and 30 days before the intended export); and
    (4) Provide reasons for the request for reduction in time.
    (d) Response to requests for reduction of time. The Assistant 
Executive Director for Compliance has the authority to approve or 
disapprove requests for reduction of time. The Assistant Executive 
Director shall indicate the amount of time before export that the 
exporter must provide the notification. If the request is not granted, 
the Assistant Executive Director shall explain the reasons in writing.



Sec. 1019.6  Changes to notification.

    If the exporter causes any change to any of the information required 
by Sec. 1019.4, or learns of any change to any of that information, at 
any time before the noncomplying goods reach the country of destination, 
the exporter must notify the Assistant Executive Director for Compliance 
within two working days after causing or learning of such change, and 
must state the reason for any such change. The Assistant Executive 
Director will promptly inform the exporter whether the 30-day advance 
notification period will be discontinued, and whether the exporter must 
take any other steps to comply with the advance notification 
requirement.



Sec. 1019.7  Commission notification of foreign governments.

    After receiving notification from the exporter, or any changes in 
notification, the Assistant Executive Director for Compliance shall 
inform on a priority basis the appropriate government agency of the 
country to which the noncomplying goods are to be sent of the 
exportation and the basis on which the goods are banned or fail to 
comply with Commission standards, regulations, or statutes, and shall 
send all information supplied by the exporter in accordance with 
Sec. 1019.4(d). The Assistant Executive Director shall also enclose any 
information supplied in accordance with Sec. 1019.4(e), but he or she 
may also state that the Commission disagrees with or takes no position 
on its content, including its relevance or accuracy. The Assistant 
Executive Director shall take whatever other action is necessary to 
provide full information to foreign countries and shall also work with 
and inform the U.S. State Department and foreign embassies and 
international organizations, as appropriate. The Assistant Executive 
Director shall also seek acknowledgment of the notification from the 
foreign government. Foreign governments intending to prohibit entry of 
goods that are the subject of a notification from the Commission should 
initiate action to prevent such entry and should notify the exporter 
directly of that intent.



Sec. 1019.8  Confidentiality.

    If the exporter believes any of the information submitted should be 
considered trade secret or confidential commercial or financial 
information, the exporter must request confidential treatment, in 
writing, at the time the information is submitted or must indicate that 
a request will be made within 10 working days. The Commission's 
regulations under the Freedom of Information Act, 16 CFR part 1015, 
govern confidential treatment of information submitted to the 
Commission.

[[Page 60]]



 Subpart B--Statement of Policy and Interpretation Concerning Export of 
              Noncomplying, Misbranded, or Banned Products



Sec. 1019.31  Purpose and scope.

    (a) This subpart B of this part 1019 states the policy of the 
Consumer Product Safety Commission and its interpretation of the 
Consumer Product Safety Act and the Federal Hazardous Substances Act 
with regard to exportation of products which have been sold, offered for 
sale, or distributed in commerce for use in the United States which:
    (1) Fail to comply with an applicable consumer product safety 
standard or banning rule issued under provisions of the Consumer Product 
Safety Act (15 U.S.C. 2051 et seq.); or
    (2) Are ``misbranded hazardous substances'' or ``banned hazardous 
substances'' as those terms are used in the Federal Hazardous Substances 
Act (15 U.S.C. 1261 et seq.).
    (b) The policy expressed in this subpart B of part 1019 does not 
apply to any of the following products:
    (1) Products which could be regulated only under provisions of the 
Consumer Product Safety Act but which are not subject to a consumer 
product safety standard or banning rule issued under that Act.
    (2) Consumer products which are subject to and fail to comply with 
an applicable standard or banning rule issued under provisions of the 
Consumer Product Safety Act but which have never been distributed in 
commerce for use in the United States. See section 18(b) of the Consumer 
Product Safety Act 15, U.S.C. 2067(b), and subpart A of this part 1019 
for requirements governing export of such products.)
    (3) Products which could be regulated under one or more sections of 
the Federal Hazardous Substances Act but which are neither ``misbranded 
hazardous substances'' nor ``banned hazardous substances'' as those 
terms are used in the Act.
    (4) Products which are ``misbranded hazardous substances'' or 
``banned hazardous substances'' as those terms are used in the Federal 
Hazardous Substances Act but which have never been sold or offered for 
sale in domestic commerce. (See sections 5(b) and 14(d) of the Federal 
Hazardous Substances Act (15 U.S.C. 1264(b) and 1273(d) and subpart A of 
this part 1019 for requirements governing export of such products.)
    (5) Products for which the Commission has granted an exemption from 
an applicable standard, ban, or labeling requirement under the CPSA, 
FHSA, or FFA, in accordance with provisions of 16 CFR 1009.9. (These 
products remain subject to the notification requirements of subpart A of 
this part 1019.)
    (6) Products which fail to comply with an applicable standard of 
flammability issued under provisions of the Flammable Fabrics Act (15 
U.S.C. 1191 et seq.). The Commission's policy regarding export of such 
products is set forth in the Commission's Memorandum Decision and Order 
In the Matter of Imperial Carpet Mills, Inc., CPSC Docket No. 80-2, July 
7, 1983, and allows export without regard to whether the products have 
been distributed in domestic commerce. (See section 15 of the Flammable 
Fabrics Act, 15 U.S.C. 1202, and subpart A of this part 1019 for 
requirements governing export of such products.)



Sec. 1019.32  Statutory provisions.

    (a) Section 18(a) of the Consumer Product Safety Act (15 U.S.C. 
2057(a)) states:
    This Act [the Consumer Product Safety Act] shall not apply to any 
consumer product if: (1) It can be shown that such product is 
manufactured, sold, or held for sale for export from the United States 
(or that such product was imported for export), unless (A) such consumer 
product is in fact distributed in commerce for use in the United States, 
or (B) the Commission determines that exportation of such product 
presents an unreasonable risk of injury to consumers within the United 
States, and (2) such consumer product when distributed in commerce, or 
any container in which it is enclosed when so distributed, bears a stamp 
or label stating that such consumer product is intended for export; 
except that this Act shall apply to any consumer product manufactured 
for sale, offered for sale, or sold for shipment to any installation of 
the United States located outside of the United States.
    (b) Section 4 of the Federal Hazardous Substances Act (15 U.S.C. 
1263) states in part:

[[Page 61]]

    The following acts and the causing thereof are hereby prohibited: 
(a) The introduction or delivery for introduction into interstate 
commerce of any misbranded hazardous substance or banned hazardous 
substance. * * * (c) The receipt in interstate commerce of any 
misbranded hazardous substance or banned hazardous substance and the 
delivery or proffered delivery thereof for pay or otherwise.
    (c) Section 5(b) of the Federal Hazardous Substances Act (15 U.S.C. 
1264(b)) provides in part:
    No person shall be subject to the penalties of this section * * * 
(3) for having violated subsection (a) or (c) of section 4 with respect 
to any hazardous substance shipped or delivered for shipment for export 
to any foreign country, in a package marked for export on the outside of 
the shipping container and labeled in accordance with the specifications 
of the foreign purchaser and in accordance with the laws of the foreign 
country, but if such hazardous substance is sold or offered for sale in 
domestic commerce, or if the Consumer Product Safety Commission 
determines that exportation of such substance presents an unreasonable 
risk of injury to persons residing within the United States, this clause 
shall not apply.



Sec. 1019.33  Statement of policy and interpretation.

    (a) In its enforcement of the Consumer Product Safety Act, the 
Commission interprets the provisions of that Act to prohibit the export 
of products which fail to comply with an applicable consumer product 
safety standard or banning rule issued under that Act if those products 
have at any time been distributed in commerce for use in the United 
States.
    (b) In its enforcement of the Federal Hazardous Substances Act, the 
Commission interprets the provisions of the Act to prohibit the export 
of products which are misbranded substances or banned hazardous 
substances as those terms are used in that Act if those products have at 
any time been sold or offered for sale in domestic commerce.



PART 1020--SMALL BUSINESS--Table of Contents




Sec.
1020.1 Why is the Commission issuing this rule?
1020.2 What is the definition of ``small business''?
1020.3 What are the qualifications and duties of the Small Business 
          Ombudsman?
1020.4 What is the Small Business Program?
1020.5 What is the Small Business Enforcement Policy?

    Authority: 5 U.S.C. 601 note.

    Source: 61 FR 52878, Oct. 9, 1996, unless otherwise noted.



Sec. 1020.1  Why is the Commission issuing this rule?

    (a) To state the Commission's policies on small businesses;
    (b) To assure that the Commission continues to treat small 
businesses fairly;
    (c) To assure that small businesses do not bear a disproportionate 
share of any burden or cost created by a Commission regulatory, 
enforcement, or other action; and
    (d) To assure that small businesses are given every opportunity to 
participate fully in the Commission's regulatory process.



Sec. 1020.2  What is the definition of ``small business''?

    As used in this part, the term small business means any entity that 
is either a small business, small organization, or small governmental 
jurisdiction, as those terms are defined at 5 U.S.C. 601(3), (4), and 
(5), respectively.



Sec. 1020.3  What are the qualifications and duties of the Small Business Ombudsman?

    (a) The Chairman will appoint a senior, full-time Commission 
employee as Small Business Ombudsman. The Ombudsman must:
    (1) Have a working knowledge of the Commission's statutes and 
regulations;
    (2) Be familiar with the industries and products that the Commission 
regulates;
    (3) Develop a working knowledge of the regulatory problems that 
small businesses experience;
    (4) Perform the Ombudsman duties in addition to, and consistently 
with, other Commission responsibilities; and
    (5) Not work in the Office of Compliance or Office of Hazard 
Identification and Reduction.
    (b) The duties of the Small Business Ombudsman will include, but not 
be limited to, the following:
    (1) Developing and implementing a program to assist small businesses 
that is consistent with Sec. 1020.4;

[[Page 62]]

    (2) Working to expedite Commission responses to small businesses and 
providing information, guidance, and technical assistance to small 
businesses;
    (3) Performing a review, at least twice a year, of the Commission's 
regulatory agenda for actions likely to have a significant impact on 
small businesses; and
    (4) Pursuing the interests of small businesses by maintaining a 
working relationship with appropriate officials in the Small Business 
Administration, in national trade associations that represent small 
businesses, and in the Commission.



Sec. 1020.4  What is the Small Business Program?

    (a) Whenever the Commission is aware of the interests of small 
businesses, it will consider those interests before taking any action 
that will likely have a significant effect on small businesses.
    (b) Small businesses may request and receive special assistance from 
the Commission, as appropriate and consistent with Commission resources. 
Examples of such assistance are:
    (1) Small businesses may contact the Small Business Ombudsman to 
obtain information about Commission statutes, regulations, or programs; 
to obtain technical assistance; to determine who in the agency has 
particular expertise that might be helpful to the small business; or to 
help expedite a small business's request.
    (2) Small businesses may request assistance from the Commission by 
using the small business extension on the Commission's hotline telephone 
system. The number is 1-800-638-2772, extension 234.
    (3) The Small Business Ombudsman will directly provide small 
businesses with the requested assistance, or will direct the small 
business to the appropriate Commission staff for help.
    (c) Whenever the Commission issues a final regulatory flexibility 
analysis for a rule, under the Regulatory Flexibility Act (5 U.S.C. 
604), the Commission will publish a compliance guide for small 
businesses. The guide will explain in easy-to-understand language what 
action a small business must take to comply with the rule.
    (d) The Commission may take other appropriate actions to assist 
small businesses, but such actions will not treat any other Commission 
constituent unfairly.



Sec. 1020.5  What is the Small Business Enforcement Policy?

    (a) When appropriate, the Commission will, subject to all applicable 
statutes and regulations and paragraph (b) of this section:
    (1) Waive or reduce civil penalties for violations of a statutory or 
regulatory requirement by a small business and/or
    (2) Consider a small business's ability to pay in determining a 
penalty assessment against that small business,
    (b) The Commission may decline to waive civil penalties or consider 
a small business's ability to pay, under paragraph (a) of this section, 
when one or more of the following circumstances applies:
    (1) The small business's violations posed serious health or safety 
threats.
    (2) The small business was subject to multiple enforcement actions 
by the Commission.
    (3) The small business's violations involved willful or criminal 
conduct.
    (4) The small business failed to correct violations within a 
reasonable time.
    (5) The small business failed to make a good faith effort to comply 
with the law.
    (6) The small business acted in any other way that would make it 
unfair or inappropriate for the Commission to provide a benefit under 
paragraph (a) of this section.



PART 1021--ENVIRONMENTAL REVIEW--Table of Contents




                           Subpart A--General

Sec.
1021.1 Purpose.
1021.2 Policy.
1021.3 Definitions.
1021.4 Overview of environmental review process for CPSC actions.
1021.5 Categories of CPSC actions.

                          Subpart B--Procedures

1021.6 Responsible official.
1021.7 Coordination of environmental review with CPSC procedures.

[[Page 63]]

1021.8 Legislative proposals.
1021.9 Public participation, notice, and comment.
1021.10 Emergencies.
1021.11 Information regarding NEPA compliance.

          Subpart C--Contents of Environmental Review Documents

1021.12 Environmental assessment.
1021.13 Finding of no significant impact.
1021.14 Environmental impact statement.

    Authority: 42 U.S.C 4321-4347; 40 CFR part 1500 et seq.

    Source: 45 FR 69434, Oct. 21, 1980, unless otherwise noted.



                           Subpart A--General



Sec. 1021.1  Purpose.

    This part contains Consumer Product Safety Commission procedures for 
review of environmental effects of Commission actions and for 
preparation of environmental impact statements (EIS) and related 
documents. These procedures supersede any Commission procedures 
previously applicable. The procedures provide for identification of 
effects of a proposed action and its alternatives on the environment; 
for assessment of the significance of these effects; for consideration 
of effects at the appropriate points in the Commission's decision-making 
process; and for preparation of environmental impact statements for 
major actions significantly affecting the environment. These procedures 
are intended to implement the Council on Environmental Quality's final 
regulations of November 29, 1978 (43 FR 55978; 40 CFR part 1500, et 
seq.) concerning agency compliance with the National Environmental 
Policy Act, as amended (NEPA) (15 U.S.C. 4321-4347 as amended by Pub. L. 
94-83, August 8, 1975).



Sec. 1021.2  Policy.

    It is the policy of the Commission to weigh and consider the effects 
upon the human environment of a proposed action and its reasonable 
alternatives. Actions will be designed to avoid or minimize adverse 
effects upon the quality of the human environment wherever practicable.



Sec. 1021.3  Definitions.

    (a) The term CPSC actions means rulemaking actions; enforcement 
actions; adjudications; legislative proposals or reports; construction, 
relocation, or renovation of CPSC facilities; decisions on petitions; 
and any other agency activity designated by the Executive Director as 
one necessitating environmental review.
    (b) The term Commission means the five Commissioners of the Consumer 
Product Safety Commission.
    (c) The term CPSC means the entire organization which bears the 
title Consumer Product Safety Commission.
    (d) The term NEPA regulations means the Council of Environmental 
Quality regulations of November 29, 1978 (43 FR 55978) for implementing 
the provisions of the National Environmental Policy Act, as amended (42 
U.S.C 4321, et. seq).
    (e) The term environmental review process refers to all activities 
associated with decisions to prepare an environmental assessment, a 
finding of no significant impact, or an environmental impact statement.
    (f) The definitions given in part 1508 of the Council's NEPA 
regulations are applicable to this part 1021 and are not repeated here.



Sec. 1021.4  Overview of environmental review process for CPSC actions.

    The environmental review process normally begins during the staff 
development of a proposed action and progresses through the following 
steps:
    (a) Environmental assessment. (Section 1508.9 of the NEPA 
regulations). The assessment is initiated along with the staff 
development of a proposal and the identification of realistic 
alternatives. The assessment shall be available to the Commission before 
the Commission votes on a proposal and its alternatives. Its purpose is 
to identify and describe foreseeable effects on the environment, if any, 
of the action and its alternatives. The assessment culminates in a 
written report. This report generally contains analyses of the same 
categories of information as would an EIS, but in a much less detailed 
fashion. (See Sec. 1021.10(a),

[[Page 64]]

below.) It contains sufficient information to form a basis for deciding 
whether effects on the environment are likely to be ``significant.'' 
(See Sec. 1508.27 of the NEPA regulations.).
    (b) Decision as to significance of effects on the environment. This 
decision is made by the Executive Director of the CPSC and is based upon 
the results of the environmental assessment as well as any other 
pertinent information. If the effects are significant, CPSC publishes in 
the Federal Register a notice of intent to prepare an environmental 
impact statement. (See Sec. 1508.22 of the NEPA regulations.) If not, a 
finding of no significant impact is prepared. (Section 1508.13 of the 
NEPA regulations.)
    (c) Finding of no significant impact. This is a written document 
which gives reasons for concluding that the effects of a proposed 
action, or its alternatives, on the environment will not be significant. 
Together with the environmental assessment, it explains the basis for 
not preparing an EIS. The finding of no significant impact is signed by 
the Executive Director. The finding of no significant impact and the 
environmental assessment accompany the proposed action throughout the 
Commission decision-making process.
    (d) Draft environmental impact statement. The content of a draft EIS 
is described in Sec. 1021.12, below. For a particular proposal, the 
breadth of issues to be discussed is determined by using the scoping 
process described in Sec. 1501.7 of the NEPA regulations. The draft EIS 
pertaining to a proposed rule is before the Commission at the time it 
considers the proposed action and is available to the public when the 
notice of proposed rulemaking is published or as soon as possible 
thereafter. In appropriate instances, the Federal Register preamble for 
a proposed rule may serve as the draft EIS. The draft EIS shall 
accompany the proposed action throughout the remainder of the Commission 
decision-making process.
    (e) Final EIS. The content of this document is described in 
Sec. 1021.12. A final EIS responds to all substantive comments on the 
draft statement. It is before the Commission when it considers a final 
action.
    (f) Supplemental statements. When CPSC makes changes in the proposed 
action that are important to environmental issues or when there is 
significant new environmental information, the Executive Director 
instructs CPSC staff to prepare supplements to either the draft or final 
EIS (See Sec. 1502.9(c) of the NEPA regulations).
    (g) Record of decision. (Sections 1505.2 and 1506.1 of the NEPA 
regulations.) At the time of a decision on a proposed action which 
involves an EIS, CPSC prepares a written record of decision explaining 
the decision and why any alternatives discussed in the EIS were 
rejected. This written record is signed by the Secretary of the 
Commission for the Commission. No action going forward on the proposal 
may be taken until the record of decision is signed and filed in the 
Office of the Secretary of the Commission.



Sec. 1021.5  Categories of CPSC actions.

    (a) There are no CPSC actions which ordinarily produce significant 
environmental effects. Therefore, there are no actions for which an 
environmental impact statement is normally required.
    (b) The following categories of CPSC actions have the potential of 
producing environmental effects and therefore, normally require 
environmental assessments but not necessarily environmental impact 
statements:
    (1) Regulatory actions dealing with health risks.
    (2) Actions requiring the destruction or disposal of large 
quantities of products or components of products.
    (3) Construction, relocation, or major renovation of CPSC 
facilities.
    (4) Recommendations or reports to Congress on proposed legislation 
that will substantially affect the scope of CPSC authority or the use of 
CPSC resources, authorize construction or razing of facilities, or 
dislocate large numbers of employees.
    (5) Enforcement actions which result in the widespread use of 
substitute products, which may present health risks.

[[Page 65]]

    (c) The following categories of CPSC actions normally have little or 
no potential for affecting the human environment; and therefore, neither 
an environmental assessment nor an environmental impact statement is 
required. (These categories are termed ``categorical exclusions'' in the 
NEPA regulations; see Sec. Sec. 1507.3(b)(2) and 1508.4):
    (1) Rules or safety standards to provide design or performance 
requirements for products, or revision, amendment, or revocation of such 
standards.
    (2) Product certification or labeling rules.
    (3) Rules requiring poison prevention packaging of products or 
exempting products from poison prevention packaging rules.
    (4) Administrative proceedings to require individual manufacturers 
to give notice of and/or to correct, repair, replace, or refund the 
purchase price of banned or hazardous products. Other administrative 
adjudications which are primarily law enforcement proceedings.
    (5) Recommendations or reports to Congress on proposed legislation 
to amend, delete or add procedural provisions to existing CPSC statutory 
authority.
    (6) Decisions on petitions for rulemaking.
    (7) Issuance of subpoenas, general orders, and special orders.
    (d) In exceptional circumstances, actions within category in 
paragraph (c) of this section (``categorical exclusions'') may produce 
effects on the human environment. Upon a determination by the Executive 
Director that a normally excluded proposed action may have such an 
effect, an environmental assessment and a finding of no significant 
impact or an environmental impact statement shall be prepared.



                          Subpart B--Procedures



Sec. 1021.6  Responsible official.

    (a) The Executive Director of the CPSC shall have the responsibility 
to ensure that the Commission's policies and procedures set forth in 
this part are carried out. He or she shall have the following specific 
powers and duties:
    (1) To ensure that CPSC environmental review is conducted in 
accordance with the NEPA regulations as well as this part 1021.
    (2) To evaluate the significance of effects of a CPSC action on the 
environment and to determine whether a finding of no significant impact 
or an EIS should be prepared.
    (3) To determine when a categorical exclusion requires environmental 
review because of exceptional circumstances indicating that the 
otherwise excluded action may produce an environmental effect.
    (4) To instruct CPSC staff to prepare supplements to either draft or 
final EIS's where there is new environmental information or when CPSC 
makes changes in a proposed action that are important to environmental 
issues.
    (5) To ensure that environmental documents are before the Commission 
at all stages of review of proposed action.
    (6) To make provisions for soliciting public comment on the 
anticipated effects on the environment of proposed CPSC actions and 
their reasonable alternatives at any stage of the environmental review 
process, whenever he or she decides that such comment will be helpful. 
The Executive Director, for example, shall have the power to require 
that provision for soliciting such comments, written or oral, be 
included in any announcement of a public hearing on proposed rulemaking 
or on the merits of a petition for rulemaking.
    (7) To call upon all resources and expertise available to CPSC to 
ensure that environmental review is accomplished through an 
interdisciplinary effort.
    (8) To delegate any of his or her powers and duties, other than 
paragraphs (a) (2) and (3) of this section, to any officer or employee 
of the CPSC.



Sec. 1021.7  Coordination of environmental review with CPSC procedures.

    (a) The Commission shall consider all relevant environmental 
documents in evaluating proposals for Commission

[[Page 66]]

action. The preparation and completion of assessments and statements 
required by this part shall be scheduled to assure that available 
environmental information is before the Commission at all appropriate 
stages of development of CPSC actions along with technical and economic 
information otherwise required. The range of alternatives discussed in 
appropriate environmental documents shall be encompassed by the range of 
alternatives considered by the Commission for an action.
    (b) An environmental assessment on a proposed rulemaking action 
requiring environmental review shall be available to the commission 
before the Commission votes on a proposed rule, and its alternatives. If 
the Executive Director determines that an EIS is needed, the draft EIS 
shall normally be before the Commission at the time it votes to publish 
a proposed rule. A final EIS shall be before the Commission when it 
considers final action on a proposed rule. Relevant environmental 
documents shall accompany the proposed rulemaking action throughout the 
Commission's decisionmaking process.
    (c) Draft EISs or findings of no significant impact together with 
environmental assessments shall be made available to the public for 
comment at the time of publication in the Federal Register of CPSC 
proposals for regulatory action requiring environmental review or 
promptly thereafter. Pursuant to Sec. 1506.10 of the NEPA regulations, 
no decision on a proposed action shall be made by the Commission until 
the later of 90 days after the Environmental Protection Agency (EPA) has 
published a notice announcing receipt of the draft EIS or 30 days after 
EPA announces receipt of the final EIS. These time periods may run 
concurrently. In addition, with regard to rulemaking for the purpose of 
protecting the public health and safety, the Commission may waive the 30 
day period and publish a decision on a final rule simultaneously with 
publication by EPA of the notice of availability.
    (d) Whenever the Commission decides to solicit offers by an outside 
person or organization to develop a proposed consumer product safety 
standard in accordance with section 7 of the Consumer Product Safety Act 
(15 U.S.C. 2056) and the Executive Director has determined that 
environmental review is needed, the Executive Director shall recommend 
to the Commission whether the ``offeror'' should perform an 
environmental assessment during development of the proposed standard. In 
making this recommendation, the Executive Director shall take into 
account the resources of the ``offeror'', including the expertise and 
money available to it. If the Commission decides that the ``offeror'' 
should perform an assessment, the agreement between the Commission and 
the offeror shall so provide. CPSC, however, shall independently 
evaluate any assessment prepared and shall take responsibility for the 
scope and content of the assessment.
    (e) CPSC adjudications are primarily law enforcement proceedings and 
therefore are not agency actions within the meaning of NEPA. (See 
Sec. 1508.18(8) of the NEPA regulations.) However, in CPSC formal 
rulemaking proceedings, all available environmental information, 
including any supplements to a draft or final EIS, shall be filed in the 
Office of the Secretary and shall be made part of the formal record of 
the proceeding.



Sec. 1021.8  Legislative proposals.

    Draft EISs on legislative proposals which may significantly affect 
the environment shall be prepared as described in Sec. 1506.8 of the 
NEPA regulations. The draft EIS, where feasible, shall accompany the 
legislative proposal or report to Congress and shall be available in 
time for Congressional hearings and deliberations. The draft EIS shall 
be forwarded to the Environmental Protection Agency in accordance with 
Sec. 1506.9 of the NEPA regulations. Comments on the legislative 
statement and CPSC's responses shall be forwarded to the appropriate 
Congressional committees.



Sec. 1021.9  Public participation, notice, and comment.

    (a) Information and comments are solicited from and provided to the 
public on anticipated environmental effects of CPSC actions as follows:

[[Page 67]]

    (1) Promptly after a decision is made to prepare a draft EIS, a 
notice of intent to prepare the draft EIS shall be published in the CPSC 
Public Calendar and in the Federal Register. The notice shall state the 
nature of the proposed action and available alternatives and shall 
describe the planned scoping process. The notice shall solicit 
information and comment by other governmental agencies and the public.
    (2) As soon as practicable after a finding of no significant impact 
is completed, a copy of the finding together with the environmental 
assessment report shall be forwarded to the Office of the Secretary of 
the Commission to be made available to the public. Any information and 
comments received from the public on the documents will be considered 
and will accompany the documents throughout the CPSC decisionmaking 
process, but comments will not ordinarily be answered individually.
    (3)(i) Upon completion of a draft EIS, a notice of its availability 
for comment should be published in the CPSC Public Calendar and in the 
Federal Register. Copies of the draft EIS shall be filed with the 
Environmental Protection Agency (EPA) in accordance with Sec. 1506.9 of 
the NEPA regulations. The length of the comment period on the draft EIS 
shall be stated in the notice of availability and on the cover of the 
draft EIS. The comment period, in accordance with Sec. 1506.10 of the 
NEPA regulations, shall be a minimum of 45 days from the date the notice 
of receipt of the draft EIS is published in the Federal Register by EPA. 
It should also be stated in the CPSC notice that comments received 
during the comment period will be addressed in the final EIS, whereas 
late comments will be considered to the extent practicable, and that all 
comments will be appended to the final EIS.
    (ii) Copies of the draft EIS shall be sent to public and private 
organizations known by CPSC to have special expertise with respect to 
the environmental effects involved, those who are known to have an 
interest in the action, and those who request an opportunity to comment. 
Also, copies shall be circulated for comment to Federal, State, and 
local agencies with jurisdiction by law and special expertise with 
respect to environmental effects involved. Part 1503 of the NEPA 
regulations shall be consulted for further details of this procedure.
    (iii) Draft EIS's shall be available to the public in the Office of 
the Secretary at Commission headquarters.
    (4) Upon completion of a final EIS, a notice of its availability in 
the Office of the Secretary, shall be published in the CPSC Public 
Calendar and if deemed appropriate, in the Federal Register. Copies of 
the final EIS shall be forwarded to EPA and one copy shall be sent to 
each entity or person who commented on the draft EIS.
    (5) A list of EIS's under preparation and of EIS's or findings of no 
significant impact and environmental assessments completed shall be 
available to the public in the Office of the Secretary, at Commission 
headquarters. The list shall be continuously updated.
    (6) In addition to publication in the CPSC Public Calendar and the 
Federal Register, notices called for by this section may also be 
publicized through press releases or local newspapers, whenever 
appropriate.



Sec. 1021.10  Emergencies.

    Where emergency circumstances make it necessary to take an action 
without observing all the provisions of these implementing procedures or 
the NEPA regulations, CPSC will consult with the Council on 
Environmental Quality about alternative arrangements.



Sec. 1021.11  Information regarding NEPA compliance.

    Interested persons may contact the Commission's Office of the 
Executive Director (301-504-0550) for information regarding CPSC NEPA 
compliance.

[45 FR 69434, Oct. 21, 1980, as amended at 62 FR 46667, Sept. 4, 1997]



          Subpart C--Contents of Environmental Review Documents



Sec. 1021.12  Environmental assessment.

    (a) An environmental assessment shall first briefly describe the 
proposed action and realistic alternative actions. Next, it shall 
identify all effects

[[Page 68]]

on the environment that can be expected to result from the proposed and 
alternative actions. After each anticipated effect is identified, it 
shall be described as fully as can be done with available data in order 
to show its magnitude and significance. Sources of information for 
assessment include CPSC staff studies and research reports, information 
gathered at hearings or meetings held to obtain the views of the public 
on the proposed action, and other information received from members of 
the public and from governmental entities.
    (b) The assessment shall identify and describe any methods or 
approaches which would avoid or minimize adverse effects on the 
environment.



Sec. 1021.13  Finding of no significant impact.

    (a) A finding of no significant impact shall cite and be attached to 
the environmental assessment upon which it is based. It shall refer to 
anticipated effects upon the environment identified in the environmental 
assessment and give the reason(s) why those effects will not be 
significant. The final paragraph of the finding shall give the reasons 
why the overall impact on the environment is not regarded as 
significant.
    (b) The signature of the Executive Director shall appear at the end 
of the finding of no significant impact.



Sec. 1021.14  Environmental impact statement.

    (a) Draft and final EIS's, unless there is a compelling reason to do 
otherwise, shall conform to the recommended format specified in 
Sec. 1502.10 of the NEPA regulations and shall contain the material 
required by Sec. Sec. 1502.11 through 1502.18 of those regulations.
    (b) It may be necessary to include in an EIS a description of 
effects which are not effects on the natural or physical environment, 
but rather are, for example, purely economic or health effects. For this 
reason, an EIS may include issues and facts that are thoroughly analyzed 
in other comprehensive CPSC documents such as hazard analyses, economic 
impact analyses, or analyses of impact on particular age groups among 
consumers. In such cases, the EIS shall not duplicate the other 
documents, but rather shall cite and summarize from them. A list of 
background documents and sources of data cited in the EIS shall appear 
at the end of every EIS.



PART 1025--RULES OF PRACTICE FOR ADJUDICATIVE PROCEEDINGS--Table of Contents




     Subpart A--Scope of Rules, Nature of Adjudicative Proceedings, 
                               Definitions

Sec.
1025.1 Scope of rules.
1025.2 Nature of adjudicative proceedings.
1025.3 Definitions.

       Subpart B--Pleadings, Form, Execution, Service of Documents

1025.11 Commencement of proceedings.
1025.12 Answer.
1025.13 Amendments and supplemental pleadings.
1025.14 Form and filing of documents.
1025.15 Time.
1025.16 Service.
1025.17 Intervention.
1025.18 Class actions.
1025.19 Joinder of proceedings.

   Subpart C--Prehearing Procedures, Motions, Interlocutory Appeals, 
                     Summary Judgments, Settlements

1025.21 Prehearing conferences.
1025.22 Prehearing briefs.
1025.23 Motions.
1025.24 Interlocutory appeals.
1025.25 Summary decisions and orders.
1025.26 Settlements.

                Subpart D--Discovery, Compulsory Process

1025.31 General provisions governing discovery.
1025.32 Written interrogatories to parties.
1025.33 Production of documents and things.
1025.34 Requests for admission.
1025.35 Depositions upon oral examination.
1025.36 Motions to compel discovery.
1025.37 Sanctions for failure to comply with discovery orders.
1025.38 Subpoenas.
1025.39 Orders requiring witnesses to testify or provide other 
          information and granting immunity.

                           Subpart E--Hearings

1025.41 General rules.
1025.42 Powers and duties of Presiding Officer.
1025.43 Evidence.
1025.44 Expert witnesses.

[[Page 69]]

1025.45 In camera materials.
1025.46 Proposed findings, conclusions and order.
1025.47 Record.
1025.48 Official docket.
1025.49 Fees.

                           Subpart F--Decision

1025.51 Initial decision.
1025.52 Adoption of initial decision.
1025.53 Appeal from initial decision.
1025.54 Review of initial decision in absence of appeal.
1025.55 Final decision on appeal or review.
1025.56 Reconsideration.
1025.57 Effective date of order.
1025.58 Reopening of proceedings.

              Subpart G--Appearances, Standards of Conduct

1025.61 Who may make appearances.
1025.62 Authority for representation.
1025.63 Written appearances.
1025.64 Attorneys.
1025.65 Persons not attorneys.
1025.66 Qualifications and standards of conduct.
1025.67 Restrictions as to former members and employees.
1025.68 Prohibited communications.

    Subpart H--Implementation of the Equal Access to Justice Act in 
              Adjudicative Proceedings With the Commission

1025.70 General provisions.
1025.71 Information required from applicant.
1025.72 Procedures for considering applications.

Appendix I to Part 1025--Suggested Form of Final Prehearing Order

    Authority: Consumer Product Safety Act (secs. 15, 20, 27 (15 U.S.C. 
2064, 2069, 2076), the Flammable Fabrics Act (sec. 5, 15 U.S.C. 1194), 
the Federal Trade Commission Act (15 U.S.C. 45)), unless otherwise 
noted.

    Source: 45 FR 29215, May 1, 1980, unless otherwise noted.



     Subpart A--Scope of Rules, Nature of Adjudicative Proceedings, 
                               Definitions



Sec. 1025.1  Scope of rules.

    The rules in this part govern procedures in adjudicative proceedings 
relating to the provisions of section 15 (c), (d), and (f) and 17(b) of 
the Consumer Product Safety Act (15 U.S.C. 2064 (c), (d), (f); 2066(b)), 
section 15 of the Federal Hazardous Substances Act (15 U.S.C. 1274), and 
sections 3 and 8(b) of the Flammable Fabrics Act (15 U.S.C. 1192, 
1197(b)), which are required by statute to be determined on the record 
after opportunity for a public hearing. These rules will also govern 
adjudicative proceedings for the assessment of civil penalties under 
section 20(a) of the Consumer Product Safety Act (15 U.S.C. 2068(a)), 
except in those instances where the matter of a civil penalty is 
presented to a United States District Court in conjunction with an 
action by the Commission for injunctive or other appropriate relief. 
These Rules may also be used for such other adjudicative proceedings as 
the Commission, by order, shall designate. A basic intent of the 
Commission in the development of these rules has been to promulgate a 
single set of procedural rules which can accommodate both simple matters 
and complex matters in adjudication. To accomplish this objective, broad 
discretion has been vested in the Presiding Officer who will hear a 
matter being adjudicated to allow him/her to alter time limitations and 
other procedural aspects of a case, as required by the complexity of the 
particular matter involved. A major concern of the Commission is that 
all matters in adjudication move forward in a timely manner, consistent 
with the Constitutional due process rights of all parties. It is 
anticipated that in any adjudicative proceedings for the assessment of 
civil penalties there will be less need for discovery since most factual 
matters will already be known by the parties. Therefore, the Presiding 
Officer should, whenever appropriate, expedite the proceedings by 
setting shorter time limitations than those time limitations generally 
applicable under these Rules. For example, the 150-day limitation for 
discovery, as provided in Sec. 1025.31(g), should be shortened, 
consistent with the extent of discovery reasonably necessary to prepare 
for the hearing.

[45 FR 29215, May 1, 1980, as amended at 47 FR 46846, Oct. 21, 1982]



Sec. 1025.2  Nature of adjudicative proceedings.

    Adjudicative proceedings shall be conducted in accordance with Title 
5, United States Code, sections 551 through 559, and these Rules. It is 
the

[[Page 70]]

policy of the Commission that adjudicative proceedings shall be 
conducted expeditiously and with due regard to the rights and interests 
of all persons affected and in locations chosen with due regard to the 
convenience of all parties. Therefore, the Presiding Officer and all 
parties shall make every effort at each stage of any proceedings to 
avoid unnecessary delay.



Sec. 1025.3  Definitions.

    As used in this part:
    (a) Application means an ex parte request by a party for an order 
that may be granted or denied without opportunity for response by any 
other party.
    (b) Commission means the Consumer Product Safety Commission or a 
quorum thereof.
    (c) Commissioner means a Commissioner of the Consumer Product Safety 
Commission.
    (d) Complaint Counsel means counsel for the Commission's staff.
    (e) Motion means a request by a party for a ruling or order that may 
be granted or denied only after opportunity for responses by all other 
parties.
    (f) Party means any named person or any intervenor in any 
proceedings governed by these Rules.
    (g) Person means any individual, partnership, corporation, 
unincorporated association, public or private organization, or a 
federal, state or municipal governmental entity.
    (h) Petition means a written request, addressed to the Commission or 
the Presiding Officer, for some affirmative action.
    (i) Presiding Officer means a person who conducts any adjudicative 
proceedings under this part, and may include an administrative law judge 
qualified under Title 5, United States Code, section 3105, but shall not 
include a Commissioner.
    (j) Respondent means any person against whom a complaint has been 
issued.
    (k) Secretary means the Secretary of the Consumer Product Safety 
Commission.
    (l) Staff means the staff of the Consumer Product Safety Commission.

Additional definitions relating to prohibited communications are in 
Sec. 1025.68.



       Subpart B--Pleadings, Form, Execution, Service of Documents



Sec. 1025.11  Commencement of proceedings.

    (a) Notice of institution of enforcement proceedings. Any 
adjudicative proceedings under this part shall be commenced by the 
issuance of a complaint, authorized by the Commission, and signed by the 
Associate Executive Director for Compliance and Enforcement.
    (b) Form and content of complaint. The complaint shall contain the 
following:
    (1) A statement of the legal authority for instituting the 
proceedings, including the specific sections of statutes, rules and 
regulations involved in each allegation.
    (2) Identification of each respondent or class of respondents.
    (3) A clear and concise statement of the charges, sufficient to 
inform each respondent with reasonable definiteness of the factual basis 
or bases of the allegations of violation or hazard. A list and summary 
of documentary evidence supporting the charges shall be attached.
    (4) A request for the relief which the staff believes is in the 
public interest.
    (c) Notice to the public. Once issued, the complaint shall be 
submitted without delay to the Federal Register for publication.



Sec. 1025.12  Answer.

    (a) Time for filing. A respondent shall have twenty (20) days after 
service of a complaint to file an answer.
    (b) Contents of answer. The answer shall contain the following:
    (1) A specific admission or denial of each allegation in the 
complaint. If a respondent is without knowledge or information 
sufficient to form a belief as to the truth of an allegation, the 
respondent shall so state. Such statement shall have the effect of a 
denial. Allegations that are not denied shall be deemed to have been 
admitted.
    (2) A concise statement of the factual or legal defenses to each 
allegation of the complaint.
    (c) Default. Failure of a respondent to file an answer within the 
time provided, unless extended, shall constitute

[[Page 71]]

a waiver of the right to appear and contest the allegations in the 
complaint, and the Presiding Officer may make such findings of fact and 
conclusions of law as are just and reasonable under the circumstances.



Sec. 1025.13  Amendments and supplemental pleadings.

    The Presiding Officer may allow appropriate amendments and 
supplemental pleadings which do not unduly broaden the issues in the 
proceedings or cause undue delay.



Sec. 1025.14  Form and filing of documents.

    (a) Filing. Except as otherwise provided in these Rules, all 
documents submitted to the Commission or the Presiding Officer shall be 
addressed to, and filed with, the Secretary. Documents may be filed in 
person or by mail and shall be deemed filed on the day of filing or 
mailing.
    (b) Caption. Every document shall contain a caption setting forth 
the name of the action, the docket number, and the title of the 
document.
    (c) Copies. An original and three (3) copies of all documents shall 
be filed. Each copy must be clear and legible.
    (d) Signature. (1) The original of each document filed shall be 
signed by a representative of record for the party or participant; or in 
the case of parties or participants not represented, by the party or 
participant; or by a partner, officer or other appropriate official of 
any corporation, partnership, or unincorporated association, who files 
an appearance on behalf of the party or participant.
    (2) By signing a document, the signer represents that the the signer 
has read it and that to the best of the signer's knowledge, information 
and belief, the statements made in it are true and that it is not filed 
for purposes of delay.
    (e) Form. (1) All documents shall be dated and shall contain the 
address and telephone number of the signer.
    (2) Documents shall be on paper approximately 8\1/2\ x 11 inches in 
size. Print shall not be less than standard elite or 12 point type. 
Pages shall be fastened in the upper left corner or along the left 
margin.
    (3) Documents that fail to comply with this section may be returned 
by the Secretary.



Sec. 1025.15  Time.

    (a) Computation. In computing any period of time prescribed or 
allowed by these rules, the day of the act, event, or default from which 
the designated period of time begins to run shall not be included. The 
last day of the period so computed shall be included, unless it is a 
Saturday, a Sunday, or a legal holiday, in which event the period runs 
until the end of the next day which is not a Saturday, a Sunday, or a 
legal holiday. When the period of time prescribed or allowed is less 
than seven (7) days, intermediate Saturdays, Sundays, and legal holidays 
shall be excluded in the computation. As used in this rule, ``legal 
holiday'' includes New Year's Day, Washington's Birthday, Memorial Day, 
Independence Day, Labor Day, Columbus Day, Veterans' Day, Thanksgiving 
Day, Christmas Day, and any other day declared as a holiday by the 
President or the Congress of the United States.
    (b) Additional time after service by mail. Whenever a party is 
required or permitted to do an act within a prescribed period after 
service of a document and the document is served by mail, three (3) days 
shall be added to the prescribed period.
    (c) Extensions. For good cause shown, the Presiding Officer may 
extend any time limit prescribed or allowed by these rules or by order 
of the Commission or the Presiding Officer, except for those sections 
governing the filing of interlocutory appeals and appeals from Initial 
Decisions and those sections expressly requiring Commission action. 
Except as otherwise provided by law, the Commission, for good cause 
shown, may extend any time limit prescribed by these rules or by order 
of the Commission or the Presiding Officer.



Sec. 1025.16  Service.

    (a) Mandatory service. Every document filed with the Secretary shall 
be served upon all parties to any proceedings, i.e., Complaint Counsel, 
respondent(s), and party intervenors, as well as the Presiding Officer. 
Every document filed with the Secretary

[[Page 72]]

shall also be served upon each participant, if the Presiding Officer or 
the Commission so directs.
    (b) Service of complaint, ruling, petition for interlocutory appeal, 
order, decision, or subpoena. A complaint, ruling, petition for 
interlocutory appeal, order, decision, or subpoena shall be served in 
one of the following ways:
    (1) By registered or certified mail. A copy of the document shall be 
addressed to the person, partnership, corporation or unincorporated 
association to be served at his/her/its residence or principal office or 
place of business and sent by registered or certified mail; or
    (2) By delivery to an individual. A copy of the document may be 
delivered to the person to be served; or to a member of the partnership 
to be served; or to the president, secretary, or other executive 
officer, or a director of the corporation or unincorporated association 
to be served; or to an agent authorized by appointment or by law to 
receive service; or
    (3) By delivery to an address. If the document cannot be served in 
person or by mail as provided in paragraph (b)(1) or (b)(2) of this 
section, a copy of the document may be left at the principal office or 
place of business of the person, partnership, corporation, 
unincorporated association, or authorized agent with an officer or a 
managing or general agent; or it may be left with a person of suitable 
age and discretion residing therein, at the residence of the person or 
of a member of the partnership or of an executive officer, director, or 
agent of the corporation or unincorporated association to be served; or
    (4) By publication in the Federal Register. A respondent that cannot 
be served by any of the methods already described in this section may be 
served by publication in the Federal Register and such other notice as 
may be directed by the Presiding Officer or the Commission, where a 
complaint has issued in a class action pursuant to Sec. 1025.18.
    (c) Service of other documents. Except as otherwise provided in 
paragraph (b) of this section, when service of a document starts the 
running of a prescribed period of time for the submission of a 
responsive document or the occurrence of an event, the document may be 
served as provided in paragraph (b) of this section or by ordinary 
first-class mail, properly addressed, postage prepaid.
    (d) Service on a representative. When a party has appeared by an 
attorney or other representative, service upon that attorney or other 
representative shall constitute service upon the party.
    (e) Certificate of service. The original of every document filed 
with the Commission and required to be served upon all parties to any 
proceedings, as well as participants if so directed by the Presiding 
Officer, shall be accompanied by a certificate of service signed by the 
party making service, stating that such service has been made upon each 
party and participant to the proceedings. Certificates of service may be 
in substantially the following form:
    I hereby certify that I have served the attached document upon all 
parties and participants of record in these proceedings by mailing, 
postage prepaid, (or by delivering in person) a copy to each on
________________________________________________________________________
________________________________________________________________________
(Signature)
For_____________________________________________________________________
    (f) Date of service. The date of service of a document shall be the 
date on which the document is deposited with the United States Postal 
Service, postage prepaid, or is delivered in person.



Sec. 1025.17  Intervention.

    (a) Participation as an intervenor. Any person who desires to 
participate as a party in any proceedings subject to these rules shall 
file a written petition for leave to intervene with the Secretary and 
shall serve a copy of the petition on each party.
    (1) A petition shall ordinarily be filed not later than the 
convening of the first prehearing conference. A petition filed after 
that time will not be granted unless the Presiding Officer determines 
that the petitioner has made a substantial showing of good cause for 
failure to file on time.
    (2) A petition shall:
    (i) Identify the specific aspect or aspects of the proceedings as to 
which the petitioner wishes to intervene,
    (ii) Set forth the interest of the petitioner in the proceedings,

[[Page 73]]

    (iii) State how the petitioner's interest may be affected by the 
results of the proceedings, and
    (iv) State any other reasons why the petitioner should be permitted 
to intervene as a party, with particular reference to the factors set 
forth in paragraph (d) of this section. Any petition relating only to 
matters outside the jurisdiction of the Commission shall be denied.
    (3) Any person whose petition for leave to intervene is granted by 
the Presiding Officer shall be known as an ``intervenor'' and as such 
shall have the full range of litigating rights afforded to any other 
party.
    (b) Participation by a person not an intervenor. Any person who 
desires to participate in the proceedings as a non-party shall file with 
the Secretary a request to participate in the proceedings and shall 
serve a copy of such request on each party to the proceedings.
    (1) A request shall ordinarily be filed not later than the 
commencement of the hearing. A petition filed after that time will not 
be granted unless the Presiding Officer determines that the person 
making the request has made a substantial showing of good cause for 
failure to file on time.
    (2) A request shall set forth the nature and extent of the person's 
alleged interest in the proceedings. Any request relating only to 
matters outside the jurisdiction of the Commission shall be denied.
    (3) Any person who files a request to participate in the proceedings 
as a non-party and whose request is granted by the Presiding Officer 
shall be known as a ``Participant'' and shall have the right to 
participate in the proceedings to the extent of making a written or oral 
statement of position, filing proposed findings of fact, conclusions of 
law and a post hearing brief with the Presiding Officer, and filing an 
appellate brief before the Commission if an appeal is taken by a party 
or review is ordered by the Commission in accordance with Sec. 1025.53 
or Sec. 1025.54, as applicable, of these rules.
    (c) Response to petition to intervene. Any party may file a response 
to a petition for leave to intervene after the petition is filed with 
the Secretary, with particular reference to the factors set forth in 
paragraph (d) of this section.
    (d) Ruling by Presiding Officer on petition. In ruling on a petition 
for leave to intervene, the Presiding Officer shall consider, in 
addition to all other relevant matters, the following factors:
    (1) The nature of the petitioner's interest, under the applicable 
statute governing the proceedings, to be made a party to the 
proceedings;
    (2) The nature and extent of the petitioner's interest in protecting 
himself/herself/itself or the public against unreasonable risks of 
injury associated with consumer products;
    (3) The nature and extent of the petitioner's property, financial or 
other substantial interest in the proceedings;
    (4) Whether the petitioner would be aggrieved by any final order 
which may be entered in the proceedings;
    (5) The extent to which the peititioner's intervention may 
reasonably be expected to assist in developing a sound record;
    (6) The extent to which the petitioner's interest will be 
represented by existing parties;
    (7) The extent to which the petitioner's intervention may broaden 
the issues or delay the proceedings; and
    (8) The extent to which the petitioner's interest can be protected 
by other available means.

If the Presiding Officer determines that a petitioner has failed to make 
a sufficient showing to be allowed to intervene as a party, the 
Presiding Officer shall view such petition to intervene as if it had 
been timely filed as a request to participate in the proceedings as a 
participant pursuant to paragraph (b) of this section.
    (e) Ruling by Presiding Officer on request. In ruling on a request 
to participate as a participant, the Presiding Officer, in the exercise 
of his/her discretion, shall be mindful of the Commission's mandate 
under its enabling legislation (see 15 U.S.C. 2051 et seq.) and its 
affirmative desire to afford interested persons, including consumers and 
consumer organizations, as well as governmental entities, an opportunity 
to participate in the agency's regulatory processes, including 
adjudicative proceedings. The Presiding Officer shall

[[Page 74]]

consider, in addition to all other relevant matters, the following 
factors:
    (1) The nature and extent of the person's alleged interest in the 
proceedings;
    (2) The possible effect of any final order which may be entered in 
the proceedings on the person's interest; and
    (3) The extent to which the person's participation can be expected 
to assist the Presiding Officer and the Commission in rendering a fair 
and equitable resolution of all matters in controversy in the 
proceedings.

The Presiding Officer may deny a request to participate if he/she 
determines that the person's participation cannot reasonably be expected 
to assist the Presiding Officer or the Commission in rendering a fair 
and equitable resolution of matters in controversy in the proceedings or 
if he/she determines that the person's participation would unduly 
broaden the issues in controversy or unduly delay the proceedings.
    (f) Designation of single representative. If the Presiding Officer 
determines that a petitioner pursuant to paragraph (a) of this section 
or a person requesting to participate pursuant to paragraph (b) of this 
section is a member of a class of prospective intervenors or 
participants, as applicable, who share an identity of interest, the 
Presiding Officer may limit such intervention or participation, as 
applicable, through designation of a single representative by the 
prospective intervenors or participants, as applicable, or, if they are 
unable to agree, by designation of the Presiding Officer.



Sec. 1025.18  Class actions.

    (a) Prerequisites to a class action. One or more members of a class 
of respondents may be proceeded against as representative parties on 
behalf of all respondents if:
    (1) The class is so numerous or geographically dispersed that 
joinder of all members is impracticable;
    (2) There are questions of fact or issues of law common to the 
class;
    (3) The defenses of the representative parties are typical of the 
defenses of the class; and
    (4) The representative parties will fairly and adequately protect 
the interests of the class.
    (b) Composition of class. A class may be composed of:
    (1) Manufacturers, distributors, or retailers, or a combination of 
them, of products which allegedly have the same defect, or
    (2) Manufacturers, distributors, or retailers, or a combination of 
them, of products which allegedly fail to conform to an applicable 
standard, regulation, or consumer product safety rule, or
    (3) Manufacturers, distributors, or retailers, or a combination of 
them, who have themselves allegedly failed to conform to an applicable 
standard, regulation, or consumer product safety rule.

When appropriate, a class may be divided into subclasses and each 
subclass shall be treated as a class.
    (c) Notice of commencement. A complaint issued under this section 
shall identify the class, the named respondents considered to be 
representative of the class, and the alleged defect or nonconformity 
common to the products manufactured, imported, distributed or sold by 
the members of the class. The complaint shall be served upon the parties 
in accordance with Sec. 1025.16.
    (d) Proper class action determination. Upon motion of Complaint 
Counsel and as soon as practicable after the commencement of any 
proceedings brought as a class action, the Presiding Officer shall 
determine by order whether the action is a proper class action. It is a 
proper class action if the prerequisites of paragraph (a) of this 
section are met and if the Presiding Officer finds that:
    (1) The prosecution of separate actions against individual members 
of the respondent class might result in (i) inconsistent or varying 
determinations with respect to individual members of the class which 
might produce incompatible or conflicting results, or (ii) 
determinations with respect to individual members of the class which 
would, as a practical matter, be dispositive of the interests of the 
other members who are not parties to the proceedings or would 
substantially impair or impede the ability of the absent members to 
protect their interests; or

[[Page 75]]

    (2) The Commission has acted on grounds generally applicable to the 
class, thereby making appropriate an order directed to the class as a 
whole.

In reaching a decision, the Presiding Officer shall consider the 
interests of members of the class in individually controlling the 
defense of separate actions, the extent and nature of any proceedings 
concerning the controversy already commenced against members of the 
class, the desirability or undesirability of concentrating the 
litigation in one adjudication, and the difficulties likely to be 
encountered in the management of a class action, as well as the benefits 
expected to result from the maintenance of a class action.
    (e) Revision of class membership. Upon motion of any party or any 
member of the class, or upon the Presiding Officer's own initiative, the 
Presiding Officer may revise the membership of the class.
    (f) Orders in conduct of class actions. In proceedings to which this 
section applies, the Presiding Officer may make appropriate orders:
    (1) Determining the course of the proceedings or prescribing 
measures to prevent undue repetition and promote the efficient 
presentation of evidence or argument;
    (2) Requiring (for the protection of the members of the class, or 
otherwise for the fair conduct of the action) that notice be given, in 
such manner as the Presiding Officer may direct, of any step in the 
action, of the extent of the proposed order, or of the opportunity for 
members to inform the Presiding Officer whether they consider the 
representation to be fair and adequate, or of the opportunity for class 
members to intervene and present defenses;
    (3) Requiring that the pleadings be amended to eliminate allegations 
concerning the representation of absent persons; or
    (4) Dealing with other procedural matters.

The orders may be combined with a prehearing order under Sec. 1025.21 of 
these rules and may be altered or amended as may be necessary.
    (g) Scope of final order. In any proceedings maintained as a class 
action, any Decision and Order of the Presiding Officer or the 
Commission under Sec. 1025.51 or Sec. 1025.55, as applicable, whether or 
not favorable to the class, shall include and describe those respondents 
whom the Presiding Officer or the Commission finds to be members of the 
class.
    (h) Notice of results. Upon the termination of any adjudication that 
has been maintained as a class action, the best notice practicable of 
the results of the adjudication shall be given to all members of the 
class in such manner as the Presiding Officer or the Commission directs.



Sec. 1025.19  Joinder of proceedings.

    Two or more matters which have been scheduled for adjudicative 
proceedings and which involve similar issues may be consolidated for the 
purpose of hearing or Commission review. A motion for consolidation may 
be filed by any party to such proceedings not later than thirty (30) 
days prior to the hearing and served upon all parties to all proceedings 
in which joinder is contemplated. The motion may include a request that 
the consolidated proceedings be maintained as a class action in 
accordance with Sec. 1025.18 of these rules. The proceedings may be 
consolidated to such extent and upon such terms as may be proper. Such 
consolidation may also be ordered upon the initiative of the Presiding 
Officer or the Commission. Single representatives may be designated by 
represented parties, intervenors, and participants with an identity of 
interests.



   Subpart C--Prehearing Procedures, Motions, Interlocutory Appeals, 
                     Summary Judgments, Settlements



Sec. 1025.21  Prehearing conferences.

    (a) When held. Except when the presiding officer determines that 
unusual circumstances would render it impractical or valueless, a 
prehearing conference shall be held in person or by conference telephone 
call within fifty (50) days after publication of the complaint in the 
Federal Register and upon ten (10) days' notice to all parties and 
participants. At the prehearing conference any or all of the following 
shall be considered:

[[Page 76]]

    (1) Petitions for leave to intervene;
    (2) Motions, including motions for consolidation of proceedings and 
for certification of class actions;
    (3) Identification, simplification and clarification of the issues;
    (4) Necessity or desirability of amending the pleadings;
    (5) Stipulations and admissions of fact and of the content and 
authenticity of documents;
    (6) Oppositions to notices of depositions;
    (7) Motions for protective orders to limit or modify discovery;
    (8) Issuance of subpoenas to compel the appearance of witnesses and 
the production of documents;
    (9) Limitation of the number of witnesses, particularly to avoid 
duplicate expert witnesses;
    (10) Matters of which official notice should be taken and matters 
which may be resolved by reliance upon the laws administered by the 
Commission or upon the Commission's substantive standards, regulations, 
and consumer product safety rules;
    (11) Disclosure of the names of witnesses and of documents or other 
physical exhibits which are intended to be introduced into evidence;
    (12) Consideration of offers of settlement;
    (13) Establishment of a schedule for the exchange of final witness 
lists, prepared testimony and documents, and for the date, time and 
place of the hearing, with due regard to the convenience of the parties; 
and
    (14) Such other matters as may aid in the efficient presentation or 
disposition of the proceedings.
    (b) Public notice. The Presiding Officer shall cause a notice of the 
first prehearing conference, including a statement of the issues, to be 
published in the Federal Register at least ten (10) days prior to the 
date scheduled for the conference.
    (c) Additional conferences. Additional prehearing conferences may be 
convened at the discretion of the Presiding Officer, upon notice to the 
parties, any participants, and to the public.
    (d) Reporting. Prehearing conferences shall be stenographically 
reported as provided in Sec. 1025.47 of these rules and shall be open to 
the public, unless otherwise ordered by the Presiding Officer or the 
Commission.
    (e) Prehearing orders. The Presiding Officer shall issue a final 
prehearing order in each case after the conclusion of the final 
prehearing conference. The final prehearing order should contain, to the 
fullest extent possible at that time, all information which is necessary 
for controlling the course of the hearing. The Presiding Officer may 
require the parties to submit a jointly proposed final prehearing order, 
such as in the format set forth in appendix I.



Sec. 1025.22  Prehearing briefs.

    Not later than ten (10) days prior to the hearing, unless otherwise 
ordered by the Presiding Officer, the parties may simultaneously serve 
and file prehearing briefs which should set forth:
    (a) A statement of the facts expected to be proved and of the 
anticipated order of proof;
    (b) A statement of the issues and the legal arguments in support of 
the party's contentions with respect to each issue; and
    (c) A table of authorities relied upon.



Sec. 1025.23  Motions.

    (a) Presentation and disposition. During the time a matter in 
adjudication is before the Presiding Officer, all motions, whether oral 
or written, except those filed under Sec. 1025.42(e), shall be addressed 
to the Presiding Officer, who shall rule upon them promptly, after 
affording an opportunity for response.
    (b) Written motions. All written motions shall state with 
particularity the order, ruling, or action desired and the reasons why 
the action should be granted. Memoranda, affidavits, or other documents 
supporting a motion shall be served and filed with the motion. All 
motions shall contain a proposed order setting forth the relief sought. 
All written motions shall be filed with the Secretary and served upon 
all parties, and all motions addressed to the Commission shall be in 
writing.
    (c) Opposition to motions. Within ten (10) days after service of any 
written motion or petition or within such

[[Page 77]]

longer or shorter time as may be designated by these Rules or by the 
Presiding Officer or the Commission, any party who opposes the granting 
of the requested order, ruling or action may file a written response to 
the motion. Failure to respond to a written motion may, in the 
discretion of the Presiding Officer, be considered as consent to the 
granting of the relief sought in the motion. Unless otherwise permitted 
by the Presiding Officer or the Commission, there shall be no reply to 
the response expressing opposition to the motion.
    (d) Rulings on motions for dismissal. When a motion to dismiss a 
complaint or a motion for other relief is granted, with the result that 
the proceedings before the Presiding Officer are terminated, the 
Presiding Officer shall issue an Initial Decision and Order in 
accordance with the provisions of Sec. 1025.51. If such a motion is 
granted as to all issues alleged in the complaint in regard to some, but 
not all, respondents or is granted as to any part of the allegations in 
regard to any or all respondents, the Presiding Officer shall enter an 
order on the record and consider the remaining issues in the Initial 
Decision. The Presiding Officer may elect to defer ruling on a motion to 
dismiss until the close of the case.



Sec. 1025.24  Interlocutory appeals.

    (a) General. Rulings of the Presiding Officer may not be appealed to 
the Commission prior to the Initial Decision, except as provided in this 
section.
    (b) Exceptions. (1) Interlocutory appeals to Commission. The 
Commission may, in its discretion, consider interlocutory appeals where 
a ruling of the Presiding Officer:
    (i) Requires the production of records claimed to be confidential;
    (ii) Requires the testimony of a supervisory official of the 
Commission other than one especially knowledgeable of the facts of the 
matter in adjudication;
    (iii) Excludes an attorney from participation in any proceedings 
pursuant to Sec. 1025.42(b);
    (iv) Denies or unduly limits a petition for intervention pursuant to 
the provisions of Sec. 1025.17.
    (2) Procedure for interlocutory appeals. Within ten (10) days of 
issuance of a ruling other than one ordering the production of records 
claimed to be confidential, any party may petition the Commission to 
consider an interlocutory appeal of a ruling in the categories 
enumerated above. The petition shall not exceed fifteen (15) pages. Any 
other party may file a response to the petition within ten (10) days of 
its service except where the order appealed from requires the production 
of records claimed to be confidential. The response shall not exceed 
fifteen (15) pages. The Commission shall decide the petition or may 
request such further briefing or oral presentation as it deems 
necessary.
    (3) If the Presiding Officer orders the production of records 
claimed to be confidential a petition for interlocutory appeal shall be 
filed within five (5) days of the entry of the order. Any opposition to 
the petition shall be filed within five (5) days of service of the 
petition. The order of the Presiding Officer shall be automatically 
stayed until five (5) days following the date of entry of the order to 
allow an affected party the opportunity to file a petition with the 
Commission for an interlocutory appeal pursuant to Sec. 1025.24(b)(2). 
If an affected party files a petition with the Commission pursuant to 
Sec. 1025.24(b)(2) within the 5-day period, the stay of the Presiding 
Officer's order is automatically extended until the Commission decides 
the petition.
    (4) Interlocutory appeals from all other rulings--(i) Grounds. 
Interlocutory appeals from all other rulings by the Presiding Officer 
may proceed only upon motion to the Presiding Officer and a 
determination by the Presiding Officer in writing that the ruling 
involves a controlling question of law or policy as to which there is 
substantial ground for differences of opinion and that an immediate 
appeal from the ruling may materially advance the ultimate termination 
of the litigation, or that subsequent review will be an inadequate 
remedy. The Presiding Officer's certification shall state the reasons 
for the determination.
    (ii) Form. If the Presiding Officer makes the determination 
described in

[[Page 78]]

paragraph (b)(4)(i) of this section, a petition for interlocutory appeal 
under this subparagraph may be filed in accordance with paragraph (b)(2) 
of this section.
    (c) Proceedings not stayed. Except as otherwise provided under this 
section, a petition for interlocutory appeal shall not stay the 
proceedings before the Presiding Officer unless the Presiding Officer or 
the Commission so orders.



Sec. 1025.25  Summary decisions and orders.

    (a) Motion. Any party may file a motion, with a supporting 
memorandum, for a Summary Decision and Order in its favor upon all or 
any of the issues in controversy. Complaint Counsel may file such a 
motion at any time after thirty (30) days following issuance of a 
complaint, and any other party may file a motion at any time after 
issuance of a complaint. Any such motion by any party shall be filed at 
least twenty (20) days before the date fixed for the adjudicative 
hearing.
    (b) Response to motion. Any other party may, within twenty (20) days 
after service of the motion, file a response with a supporting 
memorandum.
    (c) Grounds. A Summary Decision and Order shall be granted if the 
pleadings and any depositions, answers to interrogatories, admissions, 
or affidavits show that there is no genuine issue as to any material 
fact and that the moving party is entitled to a Summary Decision and 
Order as a matter of law.
    (d) Legal effect. A Summary Decision and Order upon all the issues 
being adjudicated shall constitute the Initial Decision of the Presiding 
Officer and may be appealed to the Commission in accordance with 
Sec. 1025.53 of these rules. A Summary Decision, interlocutory in 
character, may be rendered on fewer than all issues and may not be 
appealed prior to issuance of the Initial Decision.
    (e) Case not fully adjudicated on motion. A Summary Decision and 
order that does not dispose of all issues shall include a statement of 
those material facts about which there is no substantial controversy and 
of those material facts that are actually and in good faith 
controverted. The Summary Order shall direct such further proceedings as 
are appropriate.



Sec. 1025.26  Settlements.

    (a) Availability. Any party shall have the opportunity to submit an 
offer of settlement to the Presiding Officer.
    (b) Form. Offers of settlement shall be filed in camera and the form 
of a consent agreement and order, shall be signed by the respondent or 
respondent's representative, and may be signed by any other party. Each 
offer of settlement shall be accompanied by a motion to transmit the 
proposed agreement and order to the Commission. The motion shall outline 
the substantive provisions of the agreement and state reasons why it 
should be accepted by the Commission.
    (c) Contents. The proposed consent agreement and order which 
constitute the offer of settlement shall contain the following:
    (1) An admission of all jurisdictional facts;
    (2) An express waiver of further procedural steps and of all rights 
to seek judicial review or otherwise to contest the validity of the 
Commission order;
    (3) Provisions that the allegations of the complaint are resolved by 
the consent agreement and order;
    (4) A description of the alleged hazard, noncompliance, or 
violation;
    (5) If appropriate, a listing of the acts or practices from which 
the respondent shall refrain; and
    (6) If appropriate, a detailed statement of the corrective action(s) 
which the respondent shall undertake. In proceedings arising under 
Section 15 of the Consumer Product Safety Act, 15 U.S.C. 2064, this 
statement shall contain all the elements of a ``Corrective Action 
Plan,'' as outlined in the Commission's Interpretation, Policy, and 
Procedure for Substantial Product Hazards, 16 CFR part 1115.
    (d) Transmittal. The Presiding Officer may transmit to the 
Commission for decision all offers of settlement and accompanying 
memoranda that meet the requirements enumerated in paragraph (c) of this 
section. The Presiding Officer shall consider whether an offer of

[[Page 79]]

settlement is clearly frivolous, duplicative of offers previously made 
and rejected by the Commission or contrary to establish Commission 
policy. The Presiding Officer may, but need not, recommend acceptance of 
offers. Any party may object to the transmittal to the Commission of a 
proposed consent agreement by filing a response opposing the motion.
    (e) Stay of proceedings. When an offer of settlement has been agreed 
to by all parties and has been transmitted to the Commission, the 
proceedings shall be stayed until the Commission has ruled on the offer. 
When an offer of settlement has been made and transmitted to the 
Commission but has not been agreed to by all parties, the proceedings 
shall not be stayed pending Commission decision on the offer, unless 
otherwise ordered by the Presiding Officer or the Commission.
    (f) Commission ruling. The Commission shall rule upon all 
transmitted offers of settlement. If the Commission accepts the offer, 
the Commission shall issue an appropriate order, which shall become 
effective upon issuance.
    (g) Commission rejection. If the Commission rejects an offer of 
settlement, the Secretary, in writing, shall give notice of the 
Commission's decision to the parties and the Presiding Officer. If the 
proceedings have been stayed, the Presiding Officer shall promptly issue 
an order notifying the parties of the resumption of the proceedings, 
including any modifications to the schedule resulting from the stay of 
the proceedings.
    (h) Effect of rejected offer. Neither rejected offers of settlement, 
nor the fact of the proposal of offers of settlement are admissible in 
evidence.



                Subpart D--Discovery, Compulsory Process



Sec. 1025.31  General provisions governing discovery.

    (a) Applicability. The discovery rules established in this subpart 
are applicable to the discovery of information among the parties in any 
proceedings. Parties seeking information from persons not parties may do 
so by subpoena in accordance with Sec. 1025.38 of these rules.
    (b) Discovery methods. Parties may obtain discovery by one or more 
of the following methods:
    (1) Written interrogatories;
    (2) Requests for production of documents or things;
    (3) Requests for admission; or
    (4) Depositions upon oral examination.

Unless the Presiding Officer otherwise orders under paragraph (d) of 
this section, the frequency of use of these methods is not limited.
    (c) Scope of discovery. The scope of discovery is as follows:
    (1) In general. Parties may obtain discovery regarding any matter, 
not privileged, which is within the Commission's statutory authority and 
is relevant to the subject matter involved in the proceedings, whether 
it relates to the claim or defense of the party seeking discovery or to 
the claim or defense of any other party, including the existence, 
description, nature, custody, condition and location of any books, 
documents, or other tangible things and the identity and location of 
persons having knowledge of any discoverable matter. It is not ground 
for objection that the information sought will be inadmissible at the 
hearing if the information sought appears reasonably calculated to lead 
to the discovery of admissible evidence.
    (2) Privilege. Discovery may be denied or limited, or a protective 
order may be entered, to preserve the privilege of a witness, person, or 
governmental agency as governed by the Constitution, any applicable Act 
of Congress, or the principles of the common law as they may be 
interpreted by the Commission in the light of reason and experience.
    (3) Hearing preparation: materials. Subject to the provisions of 
paragraph (c)(4) of this section, a party may obtain discovery of 
documents and tangible things otherwise discoverable under paragraph 
(c)(1) of this section and prepared in anticipation of litigation or for 
hearing by or for another party or by or for that other party's 
representative (including his attorney or consultant) only upon a 
showing that the party seeking discovery has substantial need of the 
materials in the preparation of his case and that he is

[[Page 80]]

unable without unique hardship to obtain the substantial equivalent of 
the materials by other means. In ordering discovery of such materials 
when the required showing has been made, the Presiding Officer shall 
protect against disclosure of the mental impressions, conclusions, 
opinions, or legal theories of an attorney or other representative of a 
party.
    (4) Hearing preparation: experts. Discovery of facts known and 
opinions held by experts, otherwise discoverable under the provisions of 
paragraph (c)(1) of this section and acquired or developed in 
anticipation of litigation or for trial, may be obtained only as 
follows:
    (i)(A) A party may through interrogatories require any other party 
to identify each person whom the other party expects to call as an 
expert witness at trial, to state the subject matter on which the expert 
is expected to testify, to state the substance of the facts and opinions 
to which the expert is expected to testify, and to provide a summary of 
the grounds for each opinion.
    (B) Upon motion, the Presiding Officer may order further discovery 
by other means upon a showing of substantial cause and may exercise 
discretion to impose such conditions, if any, as are appropriate in the 
case.
    (ii) A party may discover facts known or opinions held by an expert 
who has been retained or specially employed by another party in 
anticipation of litigation or preparation for trial and who is not 
expected to be called as a witness at trial only upon a showing of 
exceptional circumstances under which it is impracticable for the party 
seeking discovery to obtain facts or opinions on the same subject by 
other means.
    (iii) The Presiding Officer may require as a condition of discovery 
that the party seeking discovery pay the expert a reasonable fee, but 
not more than the maximum specified in 5 U.S.C. 3109 for the time spent 
in responding to discovery.
    (d) Protective orders. Upon motion by a party and for good cause 
shown, the Presiding Officer may make any order which justice requires 
to protect a party or person from annoyance, embarrassment, competitive 
disadvantage, oppression, or undue burden or expense, including one or 
more of the following:
    (1) That the discovery shall not be had;
    (2) That the discovery may be had only on specified terms and 
conditions, including a designation of the time or place;
    (3) That the discovery shall be had only by a method of discovery 
other than that selected by the party seeking discovery;
    (4) That certain matters shall not be inquired into or that the 
scope of discovery shall be limited to certain matters;
    (5) That discovery shall be conducted with no one present except 
persons designated by the Presiding Officer;
    (6) That a trade secret or other confidential research, development, 
or commercial information shall not be disclosed or shall be disclosed 
only in a designated way or only to designated parties; and
    (7) That responses to discovery shall be placed in camera in 
accordance with Sec. 1025.45 of these rules.

If a motion for a protective order is denied in whole or in part, the 
Presiding Officer may, on such terms or conditions as are appropriate, 
order that any party provide or permit discovery.
    (e) Sequence and timing of discovery. Discovery may commence at any 
time after filing of the answer. Unless otherwise provided in these 
Rules or by order of the Presiding Officer, methods of discovery may be 
used in any sequence and the fact that a party is conducting discovery, 
whether by deposition or otherwise, shall not operate to delay any other 
party's discovery.
    (f) Supplementation of responses. A party who has responded to a 
request for discovery with a response that was complete when made is 
under a duty to supplement that response to include information later 
obtained.
    (g) Completion of discovery. All discovery shall be completed as 
soon as practical but in no case longer than one hundred fifty (150) 
days after issuance of a complaint, unless otherwise ordered by the 
Presiding Officer in exceptional circumstances and for good cause shown. 
All discovery shall be commenced by a date which affords the party from 
whom discovery is sought

[[Page 81]]

the full response period provided by these Rules.
    (h) Service and filing of discovery. All discovery requests and 
written responses, and all notices of deposition, shall be filed with 
the Secretary and served on all parties and the Presiding Officer.
    (i) Control of discovery. The use of these discovery procedures is 
subject to the control of the Presiding Officer, who may issue any just 
and appropriate order for the purpose of ensuring their timely 
completion.



Sec. 1025.32  Written interrogatories to parties.

    (a) Availability; procedures for use. Any party may serve upon any 
other party written interrogatories to be answered by the party served 
or, if the party served is a public or private corporation or a 
partnership or unincorporated association or governmental entity, by any 
officer or agent, who shall furnish such information as is available to 
the party. Interrogatories may, without leave of the Presiding Officer, 
be served upon any party after the filing of an answer.
    (b) Procedures for response. Each interrogatory shall be answered 
separately and fully in writing under oath, unless it is objected to, in 
which event the reasons for objection shall be stated in lieu of an 
answer. Each answer shall be submitted in double-spaced typewritten form 
and shall be immediately preceded by the interrogatory, in single-spaced 
typewritten form, to which the answer is responsive. The answers are to 
be signed by the person making them, and the objections signed by the 
person or representative making them. The party upon whom the 
interrogatories have been served shall serve a copy of the answers, and 
objections if any, within 30 days after service of the interrogatories. 
The Presiding Officer may allow a shorter or longer time for response. 
The party submitting the interrogatories may move for an order under 
Sec. 1025.36 of these rules with respect to any objection to, or other 
failure to answer fully, an interrogatory.
    (c) Scope of interrogatories. Interrogatories may relate to any 
matters which can be inquired into under Sec. 1025.31(c), and the 
answers may be used to any extent permitted under these rules. An 
interrogatory otherwise proper is not objectionable merely because an 
answer to the interrogatory would involve an opinion or contention which 
relates to fact or to the application of law to fact, but the Presiding 
Officer may order that such an interrogatory need not be answered until 
a later time.
    (d) Option to produce business records. Where the answer to an 
interrogatory may be derived or ascertained from the business records of 
the party upon whom the interrogatory has been served, or from an 
examination, audit, or inspection of such business records, or from a 
compilation, abstract, or summary of those records, and the burden of 
deriving the answer is substantially the same for the party serving the 
interrogatory as for the party served, it is a sufficient answer to the 
interrogatory to specify the records from which the answer may be 
derived or ascertained and to afford to the party serving the 
interrogatory reasonable opportunity to examine, audit, or inspect such 
records and to make copies, compilations, abstracts, or summaries.



Sec. 1025.33  Production of documents and things.

    (a) Scope. Any party may serve upon any other party a request:
    (1) To produce and permit the party making the request, or someone 
acting on behalf of that party, to inspect and copy any designated 
documents (including writings, drawings, graphs, charts, photographs, 
phono-records, and any other data compilation from which information can 
be obtained, translated, if necessary, by the party in possession 
through detection devices into reasonably usable form), or to inspect 
and copy, test, or sample any tangible things which constitute or 
contain matters within the scope of Sec. 1025.31(c) and which are in the 
possession, custody, or control of the party upon whom the request is 
served, or
    (2) To permit entry upon designated land or other property in the 
possession or control of the party upon whom the request is served for 
the purpose of inspection (including photographing),

[[Page 82]]

or sampling any designated object or operation within the scope of 
Sec. 1025.31(c).
    (b) Procedure for request. The request may be served at any time 
after the filing of an answer without leave of the Presiding Officer. 
The request shall set forth the items to be inspected, either by 
individual item or by category, and shall describe each item or category 
with reasonable particularity. The request shall specify a reasonable 
time, place, and manner for making the inspection and performing the 
related acts.
    (c) Procedure for response. The party upon whom the request is 
served shall respond in writing within thirty (30) days after service of 
the request. The Presiding Officer may allow a shorter or longer time 
for response. The response shall state, with respect to each item or 
category requested, that inspection and related activities will be 
permitted as requested, unless the request is objected to, in which 
event the reasons for objection shall be stated. If objection is made to 
only part of an item or category, that part shall be specified. The 
party submitting the request may move for an order under Sec. 1025.36 
with respect to any objection to or other failure to respond to the 
request or any part thereof, or to any failure to permit inspection as 
requested.
    (d) Persons not parties. This section does not preclude an 
independent action against a person not a party for production of 
documents and things.



Sec. 1025.34  Requests for admission.

    (a) Procedure for request. A party may serve upon any other party a 
written request for the admission, for the purposes of the pending 
proceedings only, of the truth of any matters within the scope of 
Sec. 1025.31(c) set forth in the request that relate to statements of 
fact or of the application of law to fact, including the genuineness of 
any documents described in the request. Copies of documents shall be 
served with the request unless they have been or are otherwise furnished 
or made available for inspection and copying. The request may, without 
leave of the Presiding Officer, be served upon any party after filing of 
the answer. Each matter about which an admission is requested shall be 
separately set forth.
    (b) Procedure for response. The matter about which an admission is 
requested will be deemed admitted unless within thirty (30) days after 
service of the request, or within such shorter or longer time as the 
Presiding Officer may allow, the party to whom the request is directed 
serves upon the party requesting the admission a written answer or 
objection addressed to the matter, signed by the party or the party's 
representative and stating the reasons for the objections. The answer 
shall specifically admit or deny the matter or set forth in detail the 
reasons why the answering party cannot truthfully admit or deny the 
matter. A denial shall fairly meet the substance of the requested 
admission. When good faith requires that a party qualify an answer or 
deny only a part of the matter to which an admission is requested, the 
party shall specify the portion that is true and qualify or deny the 
remainder. An answering party may not give lack of information or 
knowledge as a reason for failure to admit or deny a fact unless the 
party states that he/she has made reasonable inquiry and that the 
information known or readily available to him/her is insufficient to 
enable him/her to admit or deny a fact. A party who considers that a 
matter to which an admission has been requested presents a genuine issue 
for hearing may not, on that ground alone, object to the request but may 
deny the matter or set forth reasons why the party cannot admit or deny 
it. The party who has requested an admission may move to determine the 
sufficiency of any answer or objection in accordance with Sec. 1025.36 
of these Rules. If the Presiding Officer determines that an answer does 
not comply with the requirements of this section, he/she may order that 
the matter be deemed admitted or that an amended answer be served.
    (c) Effect of admission. Any matter admitted under this section is 
conclusively established unless the Presiding Officer on motion permits 
withdrawal or amendment of such admission. The Presiding Officer may 
permit withdrawal or amendment when the presentation of the merits of 
the action will be served thereby and the party who

[[Page 83]]

obtained the admission fails to satisfy the Presiding Officer that 
withdrawal or amendment will prejudice that party in maintaining an 
action or defense on the merits. Any admission made by a party under 
this section is for the purposes of the pending adjudication only and is 
not an admission by that party for any other purposes, nor may it be 
used against that party in any other proceedings.



Sec. 1025.35  Depositions upon oral examination.

    (a) When depositions may be taken. At any time after the first 
prehearing conference, upon leave of the Presiding Officer and under 
such terms and conditions as the Presiding Officer may prescribe, any 
party may take the deposition of any other party, including the agents, 
employees, consultants, or prospective witnesses of that party at a 
place convenient to the deponent. The attendance of witnesses and the 
production of documents and things at the deposition may be compelled by 
subpoena as provided in Sec. 1025.38 of these rules.
    (b) Notice of deposition--(1) Deposition of a party. A party 
desiring to take a deposition of another party to the proceedings shall, 
after obtaining leave from the Presiding Officer, serve written notice 
of the deposition on all other parties and the Presiding Officer at 
least ten (10) days before the date noticed for the deposition. The 
notice shall state:
    (i) The time and place for the taking of the deposition;
    (ii) The name and address of each person to be deposed, if known, or 
if the name is not known, a general description sufficient to identify 
him/her; and
    (iii) The subject matter of the expected testimony. If a subpoena 
duces tecum is to be served on the person to be deposed, the designation 
of the materials to be produced, as set forth in the subpoena, shall be 
attached to or included in the notice of deposition.
    (2) Deposition of a non-party. A party desiring to take a deposition 
of a person who is not a party to the proceedings shall make application 
for the issuance of a subpoena, in accordance with Sec. 1025.38 of these 
rules, to compel the attendance, testimony, and/or production of 
documents by such non-party. The paty desiring such deposition shall 
serve written notice of the deposition on all other parties to the 
proceedings, after issuance of the subpoena. The date specified in the 
subpoena for the deposition shall be at least twenty (20) days after the 
date on which the application for the subpoena is made to the Presiding 
Officer.
    (3) Opposition to notice. A person served with a notice of 
deposition may oppose, in writing, the taking of the deposition within 
five (5) days of service of the notice. The Presiding Officer shall rule 
on the notice and any opposition and may order the taking of all noticed 
depositions upon a showing of good cause. The Presiding Officer may, for 
good cause shown, enlarge or shorten the time for the taking of a 
deposition.
    (c) Persons before whom depositions may be taken. Depositions may be 
taken before any person who is authorized to administer oaths by the 
laws of the United States or of the place where the examination is held. 
No deposition shall be taken before a person who is a relative, 
employee, attorney, or representative of any party, or who is a relative 
or employee of such attorney or representative, or who is financially 
interested in the action.
    (d) Taking of deposition--(1) Examination. Each deponent shall 
testify under oath, and all testimony shall be recorded. All parties or 
their representatives may be present and participate in the examination. 
Evidence objected to shall be taken subject to any objection. Objections 
shall include the grounds relied upon. The questions and answers, 
together with all objections made, shall be recorded by the official 
reporter before whom the deposition is taken. The original or a verified 
copy of all documents and things produced for inspection during the 
examination of the deponent shall, upon a request of any party present, 
be marked for identification and made a part of the record of the 
deposition.
    (2) Motion to terminate or limit examination. At any time during the 
deposition, upon motion of any party or of the deponent, and upon a 
showing that the examination is being conducted in

[[Page 84]]

bad faith or in such manner as unreasonably to annoy, embarrass or 
oppress the deponent or party, the Presiding Officer may order the party 
conducting the examination to stop the deposition or may limit the scope 
and manner of taking the deposition as provided in Sec. 1025.31(d) of 
these rules.
    (3) Participation by parties not present. In lieu of attending a 
deposition, any party may serve written questions in a sealed envelope 
on the party conducting the deposition. That party shall transmit the 
envelope to the official reporter, who shall unseal it and read the 
questions to the deponent.
    (e) Transcription and filing of depositions--(1) Transcription. Upon 
request by any party, the testimony recorded at a deposition shall be 
transcribed. When the testimony is fully transcribed, the deposition 
shall be submitted to the deponent for examination and signature and 
shall be read to or by the deponent, unless such examination and 
signature are waived by the deponent. Any change in form or substance 
which the deponent desires to make shall be entered upon the deposition 
by the official reporter with a statement of the reasons given by the 
deponent for making them. The deposition shall then be signed by the 
deponent, unless the deponent waives signature or is ill or cannot be 
found or refuses to sign. If the deposition is not signed by the 
deponent within thirty (30) days of its submission to him/her, the 
official reporter shall sign the deposition and state on the record the 
fact of the waiver of signature or of the illness or absence of the 
deponent or of the refusal to sign, together with a statement of the 
reasons therefor. The deposition may then be used as fully as though 
signed, in accordance with paragraph (i) of this section.
    (2) Certification and filing. The official reporter shall certify on 
the deposition that it was taken under oath and that the deposition is a 
true record of the testimony given and corrections made by the deponent. 
The official reporter shall then seal the deposition in an envelope 
endorsed with the title and docket number of the action and marked 
``Deposition of [name of deponent]'' and shall promptly file the 
deposition with the Secretary. The Secretary shall notify all parties of 
the filing of the deposition and shall furnish a copy of the deposition 
to any party or to the deponent upon payment of reasonable charges.
    (f) Costs of deposition. The party who notices the deposition shall 
pay for the deposition. The party who requests transcription of the 
deposition shall pay for the transcription.
    (g) Failure to attend or to serve subpoena; expenses. If a party who 
notices a deposition fails to attend or conduct the deposition, and 
another party attends in person or by a representative pursuant to the 
notice, the Presiding Officer may order the party who gave the notice to 
pay to the attending party the reasonable expenses incurred. If a party 
who notices a deposition fails to serve a subpoena upon the deponent and 
as a result the deponent does not attend, and if another party attends 
in person or by a representative because that party expects the 
deposition to be taken, the Presiding Officer may order the party who 
gave notice to pay to the attending party the reasonable expenses 
incurred.
    (h) Deposition to preserve testimony--(1) When available. By leave 
of the Presiding Officer, a party may take the deposition of his/her own 
witness for the purpose of perpetuating the testimony of that witness. A 
party who wishes to conduct such a deposition shall obtain prior leave 
of the Presiding Officer by filing a motion. The motion shall include a 
showing of substantial reason to believe that the testimony could not be 
presented at the hearing. If the Presiding Officer is satisfied that the 
perpetuation of the testimony may prevent a failure of justice or is 
otherwise reasonably necessary, he/she shall order that the deposition 
be taken.
    (2) Procedure. Notice of a deposition to preserve testimony shall be 
served at least fifteen (15) days prior to the deposition unless the 
Presiding Officer authorizes less notice when warranted by extraordinary 
circumstances. The deposition shall be taken in accordance with the 
provisions of paragraph (d) of this section. Any deposition taken to 
preserve testimony shall be transcribed and filed in accordance with 
paragraph (e) of this section.

[[Page 85]]

    (i) Use of depositions. At the hearing or upon a petition for 
interlocutory appeal, any part or all of a deposition may be used 
against any party who was present or represented at the deposition or 
who had reasonable notice of the deposition, in accordance with any of 
the following:
    (1) Any deposition may be used by any party for the purpose of 
contradicting or impeaching the testimony of the deponent as a witness.
    (2) The deposition of anyone who at the time of the taking of the 
deposition was an officer, director, managing agent, or person otherwise 
designated to testify on behalf of a public or private corporation, 
partnership or unincorporated association or governmental entity which 
is a party to the proceedings, may be used by any adverse party for any 
purpose.
    (3) The deposition of a witness may be used by any party for any 
purpose if the Presiding Officer finds:
    (i) That the witness is dead; or
    (ii) That the witness is out of the United States, unless it appears 
that the absence of the witness was procured by the party offering the 
deposition; or
    (iii) That the witness is unable to attend or testify because of 
age, illness, infirmity, or imprisonment; or
    (iv) That the party offering the depostion has been unable to 
procure the attendance of the witness by subpoena; or
    (v) That such exceptional circumstances exist as to make it 
desirable, in the interest of justice and with due regard for the 
importance of presenting the testimony of witnesses orally during the 
hearing, to allow the deposition to be used.
    (4) If only part of a deposition is offered in evidence by a party, 
any other party may move to introduce any other part of the deposition.



Sec. 1025.36  Motions to compel discovery.

    If a party fails to respond to discovery, in whole or in part, the 
party seeking discovery may move within twenty (20) days for an order 
compelling an answer, or compelling inspection or production of 
documents, or otherwise compelling discovery. For purposes of this 
section, an evasive or incomplete response is to be treated as a failure 
to respond. When taking depositions, the discovering party shall 
continue the examination to the extent possible with respect to other 
areas of inquiry before moving to compel discovery.



Sec. 1025.37  Sanctions for failure to comply with discovery orders.

    If a party fails to obey an order to provide or permit discovery, 
the Presiding Officer may take such action as is just, including but not 
limited to the following:
    (a) Infer that the admission, testimony, document or other evidence 
would have been adverse to the party;
    (b) Order that for the purposes of the proceedings, the matters 
regarding which the order was made or any other designated facts shall 
be taken to be established in accordance with the claim of the party 
obtaining the order;
    (c) Order that the party withholding discovery not introduce into 
evidence or otherwise rely, in support of any claim or defense, upon the 
documents or other evidence withheld;
    (d) Order that the party withholding discovery not introduce into 
evidence, or otherwise use at the hearing, information obtained in 
discovery;
    (e) Order that the party withholding discovery forfeit its right to 
object to introduction and use of secondary evidence to show what the 
withheld admission, testimony, documents, or other evidence would have 
shown;
    (f) Order that a pleading, or part of a pleading, or a motion or 
other submission by the party, concerning which the order was issued, be 
stricken, or that decision on the pleadings be rendered against the 
party, or both; and
    (g) Exclude the party or representative from the proceedings, in 
accordance with Sec. 1025.42(b) of these rules.

Any such action may be taken by order at any point in the proceedings.



Sec. 1025.38  Subpoenas.

    (a) Availability. A subpoena shall be addressed to any person not a 
party for the purpose of compelling attendance, testimony, and 
production of documents at a hearing or deposition, and may be addressed 
to any party for the same purposes.

[[Page 86]]

    (b) Form. A subpoena shall identify the action with which it is 
connected; shall specify the person to whom it is addressed and the 
date, time, and place for compliance with its provisions; and shall be 
issued by order of the Commission and signed by the Secretary or by the 
Presiding Officer. A subpoena duces tecum shall specify the books, 
papers, documents, or other materials or data-compilations to be 
produced.
    (c) How obtained--(1) Content of application. An application for the 
issuance of a subpoena, stating reasons, shall be submitted in 
triplicate to the Presiding Officer. The Presiding Officer shall bring 
the application to the attention of the Commission by forwarding it or 
by communicating its contents by any other means, e.g., by telephone, to 
the Commission.
    (2) Procedure for application. The original and two copies of the 
subpoena, marked ``original,'' ``duplicate'' and ``triplicate,'' shall 
accompany the application. The Commission shall rule upon an application 
for a subpoena ex parte, by issuing the subpoena or by issuing an order 
denying the application.
    (d) Issuance of a subpoena. The Commission shall issue a subpoena by 
authorizing the Secretary or the Presiding Officer to sign and date each 
copy in the lower right-hand corner. The ``duplicate'' and 
``triplicate'' copies of the subpoena shall be transmitted to the 
applicant for service in accordance with these Rules; the ``original'' 
shall be retained by, or be forwarded to, the Secretary for retention in 
the docket of the proceedings.
    (e) Service of a subpoena. A subpoena may be served in person or by 
registered or certified mail, return receipt requested, as provided in 
Sec. 1025.16(b) of these rules. Service shall be made by delivery of the 
signed ``duplicate'' copy to the person named therein.
    (f) Return of service. A person serving a subpoena shall promptly 
execute a return of service, stating the date, time, and manner of 
service. If service is effected by mail, the signed return receipt shall 
accompany the return of service. In case of failure to make service, a 
statement of the reasons for the failure shall be made. The 
``triplicate'' copy of the subpoena, bearing or accompanied by the 
return of service, shall be returned without delay to the Secretary 
after service has been completed.
    (g) Motion to quash or limit subpoena. Within five (5) days of 
receipt of a subpoena, the person to whom it is directed may file a 
motion to quash or limit the subpoena, setting forth the reasons why the 
subpoena should be withdrawn or why it should be limited in scope. Any 
such motion shall be answered within five (5) days of service and shall 
be ruled on immediately. The order shall specify the date, if any, for 
compliance with the specifications of the subpoena.
    (h) Consequences of failure to comply. In the event of failure by a 
person to comply with a subpoena, the Presiding Officer may take any of 
the actions enumerated in Sec. 1025.37 of these rules, or may order any 
other appropriate relief to compensate for the withheld testimony, 
documents, or other materials. If in the opinion of the Presiding 
Officer such relief is insufficient, the Presiding Officer shall certify 
to the Commission a request for judicial enforcement of the subpoena.



Sec. 1025.39  Orders requiring witnesses to testify or provide other information and granting immunity.

    (a) Applicability to Flammable Fabrics Act only. This section 
applies only to proceedings arising under the Flammable Fabrics Act.
    (b) Procedure. A party who desires the issuance of an order 
requiring a witness or deponent to testify or provide other information 
upon being granted immunity from prosecution under title 18, United 
States Code, section 6002, may make a motion to that effect. The motion 
shall be made and ruled on in accordance with Sec. 1025.23 of these 
rules and shall include a showing:
    (1) That the testimony or other information sought from a witness or 
deponent, or prospective witness or deponent, may be necessary to the 
public interest; and
    (2) That such individual has refused or is likely to refuse to 
testify or provide such information on the basis of that individual's 
privilege against self-incrimination.

[[Page 87]]

    (c) Approval of the Attorney General. If the Presiding Officer 
determines that the witness' testimony appears necessary and that the 
privilege against self-incrimination may be invoked, he/she may certify 
to the Commission a request that it obtain the approval of the Attorney 
General of the United States for the issuance of an order granting 
immunity.
    (d) Issuance of order granting immunity. Upon application to and 
approval by the Attorney General of the United States, and after the 
witness has invoked the privilege against self-incrimination, the 
Presiding Officer shall issue the order granting immunity unless he/she 
determines that the privilege was improperly invoked.
    (e) Sanctions for failure to testify. Failure of a witness to 
testify after a grant of immunity or after a denial of a motion for the 
issuance of an order granting immunity shall result in the imposition of 
appropriate sanctions as provided in Sec. 1025.37 of these rules.



                           Subpart E--Hearings



Sec. 1025.41  General rules.

    (a) Public hearings. All hearings conducted pursuant to these Rules 
shall be public unless otherwise ordered by the Commission or the 
Presiding Officer.
    (b) Prompt completion. Hearings shall proceed with all reasonable 
speed and, insofar as practicable and with due regard to the convenience 
of the parties, shall continue without suspension until concluded, 
except in unusual circumstances or as otherwise provided in these Rules.
    (c) Rights of parties. Every party shall have the right of timely 
notice and all other rights essential to a fair hearing, including, but 
not limited to, the rights to present evidence, to conduct such cross-
examination as may be necessary for a full and complete disclosure of 
the facts, and to be heard by objection, motion, brief, and argument.
    (d) Rights of participants. Every participant shall have the right 
to make a written or oral statement of position and to file proposed 
findings of fact, conclusions of law, and a post hearing brief, in 
accordance with Sec. 1025.17(b) of these Rules.
    (e) Rights of witnesses. Any person compelled to testify in any 
proceedings in response to a subpoena may be accompanied, represented, 
and advised by legal counsel or other representative, and may purchase a 
transcript of his/her testimony.



Sec. 1025.42  Powers and duties of Presiding Officer.

    (a) General. A Presiding Officer shall have the duty to conduct 
full, fair, and impartial hearings, to take appropriate action to avoid 
unnecessary delay in the disposition of proceedings, and to maintain 
order. He/she shall have all powers necessary to that end, including the 
following powers:
    (1) To administer oaths and affirmations;
    (2) To compel discovery and to impose appropriate sanctions for 
failure to make discovery;
    (3) To rule upon offers of proof and receive relevant, competent, 
and probative evidence;
    (4) To regulate the course of the proceedings and the conduct of the 
parties and their representatives;
    (5) To hold conferences for simplification of the issues, settlement 
of the proceedings, or any other proper purposes;
    (6) To consider and rule, orally or in writing, upon all procedural 
and other motions appropriate in adjudicative proceedings;
    (7) To issue Summary Decisions, Initial Decisions, Recommended 
Decisions, rulings, and orders, as appropriate;
    (8) To certify questions to the Commission for its determination; 
and
    (9) To take any action authorized by these Rules or the provisions 
of title 5, United States Code, sections 551-559.
    (b) Exclusion of parties by Presiding Officer. A Presiding Officer 
shall have the authority, for good cause stated on the record, to 
exclude from participation in any proceedings any party, participant, or 
representative who violates the requirements of Sec. 1025.66 of these 
rules. Any party, participant or representative so excluded may appeal 
to the Commission in accordance with the provisions of Sec. 1025.24 of 
these rules. If the representative of a party or participant is 
excluded, the hearing may be

[[Page 88]]

suspended for a reasonable time so that the party or participant may 
obtain another representative.
    (c) Substitution of Presiding Officer. In the event of the 
substitution of a new Presiding Officer for the one originally 
designated, any motion predicated upon such substitution shall be made 
within five (5) days.
    (d) Interference. In the performance of adjudicative functions, a 
Presiding Officer shall not be responsible to or subject to the 
supervision or direction of any Commissioner or of any officer, 
employee, or agent engaged in the performance of investigative or 
prosecuting functions for the Commission. All directions by the 
Commission to a Presiding Officer concerning any adjudicative 
proceedings shall appear on and be made a part of the record.
    (e) Disqualification of Presiding Officer. (1) When a Presiding 
Officer considers himself/herself disqualified to preside in any 
adjudicative proceedings, he/she shall withdraw by notice on the record 
and shall notify the Chief Administrative Law Judge and the Secretary of 
such withdrawal.
    (2) Whenever, for good and reasonable cause, any party considers the 
Presiding Officer to be disqualified to preside, or to continue to 
preside, in any adjudicative proceedings, that party may file with the 
Secretary a motion to disqualify and remove, supported by affidavit(s) 
setting forth the alleged grounds for disqualification. A copy of the 
motion and supporting affidavit(s) shall be served by the Secretary on 
the Presiding Officer whose removal is sought. The Presiding Officer 
shall have ten (10) days to respond in writing to such motion. However, 
the motion shall not stay the proceedings unless otherwise ordered by 
the Presiding Officer or the Commission. If the Presiding Officer does 
not disqualify himself/herself, the Commission shall determine the 
validity of the grounds alleged, either directly or on the report of 
another Presiding Officer appointed to conduct a hearing for that 
purpose and, in the event of disqualification, shall take appropriate 
action by assigning another Presiding Officer or requesting loan of 
another Administrative Law Judge through the U.S. Office of Personnel 
Management.



Sec. 1025.43  Evidence.

    (a) Applicability of Federal Rules of Evidence. Unless otherwise 
provided by statute or these rules, the Federal Rules of Evidence shall 
apply to all proceedings held pursuant to these Rules. However, the 
Federal Rules of Evidence may be relaxed by the Presiding Officer if the 
ends of justice will be better served by so doing.
    (b) Burden of proof. (1) Complaint counsel shall have the burden of 
sustaining the allegations of any complaint.
    (2) Any party who is the proponent of a legal or factual proposition 
shall have the burden of sustaining that proposition.
    (c) Admissibility. All relevant and reliable evidence is admissible, 
but may be excluded by the Presiding Officer if its probative value is 
substantially outweighed by unfair prejudice or confusion of the issues, 
or by considerations of undue delay, waste of time, immateriality, or 
needless presentation of cumulative evidence.
    (d) Official notice--(1) Definition. Official notice means use by 
the Presiding Officer or the Commission of facts not appearing on the 
record and legal conclusions drawn from those facts. An officially 
noticed fact or legal conclusion must be one not subject to reasonable 
dispute in that it is either:
    (i) Generally known within the jurisdiction of the Commission or
    (ii) Capable of accurate and ready determination by resort to 
sources whose accuracy cannot reasonably be questioned.
    (2) Method of taking official notice. The Presiding Officer and/or 
the Commission may at any time take official notice upon motion of any 
party or upon its own initiative. The record shall reflect the facts and 
conclusions which have been officially noticed.
    (e) [Reserved]
    (f) Offer of proof. When an objection to proffered testimony or 
documentary evidence is sustained, the sponsoring party may make a 
specific offer, either in writing or orally, of what the party expects 
to prove by the testimony or the document. When an offer of proof is 
made, any other party may make a specific offer, either in writing or 
orally, of what the party expects to present

[[Page 89]]

to rebut or contradict the offer of proof. Written offers of proof or of 
rebuttal, adequately marked for identification, shall accompany the 
record and be available for consideration by any reviewing authority.



Sec. 1025.44  Expert witnesses.

    (a) Definition. An expert witness is one who, by reason of 
education, training, experience, or profession, has peculiar knowledge 
concerning the subject matter to which his/her testimony relates and 
from which he/she may draw inferences based upon hypothetically stated 
facts or offer opinions from facts involving scientific or technical 
knowledge.
    (b) Method of presenting testimony of expert witness. Except as may 
otherwise be ordered by the Presiding Officer, the direct testimony of 
an expert witness shall be in writing and shall be filed on the record 
and exchanged between the parties no later than ten (10) days preceding 
the commencement of the hearing. The written testimony of an expert 
witness shall be incorporated into the record and shall constitute the 
direct testimony of that witness. Upon a showing of good cause, the 
party sponsoring the expert witness may be permitted to amplify the 
written direct testimony during the hearing.
    (c) Cross-examination and redirect examination of expert witness. 
Cross-examination, redirect examination, and re-cross-examination of an 
expert witness shall proceed in due course based upon the written 
testimony and any amplifying oral testimony.
    (d) Failure to file or exchange written testimony. Failure to file 
or exchange written testimony of expert witnesses as provided in this 
section shall deprive the sponsoring party of the use of the expert 
witness and of the conclusions which that witness would have presented, 
unless the opposing parties consent or the Presiding Officer otherwise 
orders in unusual circumstances.



Sec. 1025.45  In camera materials.

    (a) Definition. In camera materials are documents, testimony, or 
other data which by order of the Presiding Officer or the Commission are 
kept confidential and excluded from the public record.
    (b) In camera treatment of documents and testimony. The Presiding 
Officer or the Commission shall have authority, when good cause is found 
on the record, to order documents or testimony offered in evidence, 
whether admitted or rejected, to be received and preserve in camera. The 
order shall specify the length of time for in camera treatment and shall 
include:
    (1) A description of the documents or testimony;
    (2) The reasons for granting in camera treatment for the specified 
length of time; and
    (3) The terms and conditions imposed by the Presiding Official, if 
any, limiting access to or use of the in camera material.
    (c) Access and disclosure to parties. (1) Commissioners and their 
staffs, Presiding Officers and their staffs, and Commission staff 
members concerned with judicial review shall have complete access to in 
camera materials. Any party to the proceedings may seek access only in 
accordance with paragraph (c)(2) of this section.
    (2) Any party desiring access to, or disclosure of, in camera 
materials for the preparation and presentation of that party's case 
shall make a motion which sets forth its justification. The Presiding 
Officer or the Commission may grant such motion for good cause shown and 
shall enter a protective order prohibiting unnecessary disclosure and 
requiring any other necessary safeguards. The Presiding Officer or the 
Commission may examine the in camera materials and excise any portions 
prior to disclosure of the materials to the moving party.
    (d) Segregation of in camera materials. In camera materials shall be 
segregated from the public record and protected from public view.
    (e) Public release of in camera materials. In camera materials 
constitute a part of the confidential records of the Commission and 
shall not be released to the public until the expiration of in camera 
treatment.
    (f) Reference to in camera materials. In the submission of proposed 
findings, conclusions, briefs, or other documents, all parties shall 
refrain from disclosing specific details of in camera materials. 
However, such refraining

[[Page 90]]

shall not preclude general references to such materials. To the extent 
that parties consider necessary the inclusion of specific details of in 
camera materials, those references shall be incorporated into separate 
proposed findings, conclusions, briefs, or other documents marked 
``Confidential, Contains In Camera Material,'' which shall be placed in 
camera and become part of the in camera record. Those documents shall be 
served only on parties accorded access to the in camera materials by 
these rules, the Presiding Officer, or the Commission.



Sec. 1025.46  Proposed findings, conclusions, and order.

    Within a reasonable time after the closing of the record and receipt 
of the transcript, all parties and participants may file, simultaneously 
unless otherwise directed by the Presiding Officer, post-hearing briefs, 
including proposed findings of fact and conclusions of law, as well as a 
proposed order. The Presiding Officer shall establish a date certain for 
the filing of the briefs, which shall not exceed fifty (50) days after 
the closing of the record except in unusual circumstances. The briefs 
shall be in writing and shall be served upon all parties. The briefs of 
all parties shall contain adequate references to the record and 
authorities relied upon. Replies shall be filed within fifteen (15) days 
of the date for the filing of briefs unless otherwise established by the 
Presiding Officer. The parties and participants may waive either or both 
submissions.



Sec. 1025.47  Record.

    (a) Reporting and transcription. Hearings shall be recorded and 
transcribed by the official reporter of the Commission under the 
supervision of the Presiding Officer. The original transcript shall be a 
part of the record of proceedings. Copies of transcripts are available 
from the reporter at a cost not to exceed the maximum rates fixed by 
contract between the Commission and the reporter. In accordance with 
Section 11 of the Federal Advisory Committee Act (Pub. L. 92-463, 5 
U.S.C. appendix I), copies of transcripts may be made by members of the 
public or by Commission personnel, when available, at the Office of the 
Secretary at reproduction costs as provided in Sec. 1025.49.
    (b) Corrections. Corrections of the official transcript may be made 
only when they involve errors affecting substance and then only in the 
manner described in this section. The Presiding Officer may order 
corrections, either on his/her own motion or on motion of any party. The 
Presiding Officer shall determine the corrections to be made and shall 
so order. Corrections shall be interlineated or otherwise inserted in 
the official transcript so as not to obliterate the original text.



Sec. 1025.48  Official docket.

    The official docket in any adjudicatory proceedings shall be 
maintained in the Office of the Secretary and be available for public 
inspection during normal business hours of the Commission.



Sec. 1025.49  Fees.

    (a) Fees for deponents and witnesses. Any person compelled to appear 
in person in response to a subpoena or notice of deposition shall be 
paid the same attendance and mileage fees as are paid witnesses in the 
courts of the United States, in accordance with title 28, United States 
Code, section 1821. The fees and mileage referred to in this paragraph 
shall be paid by the party at whose instance deponents or witnesses 
appear.
    (b) Fees for production of records. Fees charged for production or 
disclosure of records contained in the official docket shall be in 
accordance with the Commission's ``Procedures for Disclosures or 
Production of Information Under the Freedom of Information Act,'' title 
16, Code of Federal Regulations, Sec. 1015.9.



                           Subpart F--Decision



Sec. 1025.51  Initial decision.

    (a) When filed. The Presiding Officer shall endeavor to file an 
Initial Decision with the Commission within sixty (60) days after the 
closing of the record or the filing of post-hearing briefs, whichever is 
later.
    (b) Content. The Initial Decision shall be based upon a 
consideration of the

[[Page 91]]

entire record and shall be supported by reliable, probative, and 
substantial evidence. The Initial Decision shall include:
    (1) Findings and conclusions, as well as the reasons or bases for 
such findings and conclusions, upon the material questions of fact, 
material issues of law, or discretion presented on the record, and 
should, where practicable, be accompanied by specific page citations to 
the record and to legal and other materials relied upon; and
    (2) An appropriate order.
    (c) By whom made. The Initial Decision shall be made and filed by 
the Presiding Officer who presided over the hearing, unless otherwise 
ordered by the Commission.
    (d) Reopening of proceedings by Presiding Officer; termination of 
jurisdiction. (1) At any time prior to, or concomitant with, the filing 
of the Initial Decision, the Presiding Officer may reopen the 
proceedings for the reception of further evidence.
    (2) Except for the correction of clerical errors, or where the 
proceeding is reopened by an order under paragraph (d)(1) of this 
section, the jurisdiction of the Presiding Officer is terminated upon 
the filing of the Initial Decision, unless and until such time as the 
matter may be remanded to the Presiding Officer by the Commission.



Sec. 1025.52  Adoption of initial decision.

    The Initial Decision and Order shall become the Final Decision and 
Order of the Commission forty (40) days after issuance unless an appeal 
is noted and perfected or unless review is ordered by the Commission. 
Upon the expiration of the fortieth day, the Secretary shall prepare, 
sign, and enter an order adopting the Initial Decision and Order, unless 
otherwise directed by the Commission.



Sec. 1025.53  Appeal from initial decision.

    (a) Who may file notice of intention. Any party may appeal an 
Initial Decision to the Commission, provided that within ten (10) days 
after issuance of the Initial Decision such party files and serves a 
notice of intention to appeal.
    (b) Appeal brief. An appeal is perfected by filing a brief within 
forty (40) days after service of the Initial Decision. The appeal brief 
must be served upon all parties. The appeal brief shall contain, in the 
order indicated, the following:
    (1) A subject index of the matters in the brief, with page 
references, and a table of cases (alphabetically arranged), textbooks, 
statutes, and other material cited, with page references thereto;
    (2) A concise statement of the case;
    (3) A statement containing the reasons why the party believes the 
Initial Decision is incorrect;
    (4) The argument, presenting clearly the points of fact and law 
relied upon to support each reason why the Initial Decision is 
incorrect, with specific page references to the record and the legal or 
other material relied upon; and
    (5) A proposed form of order for the Commission's consideration in 
lieu of the order contained in the Initial Decision.
    (c) Answering brief. Within thirty (30) days after service of the 
appeal brief upon all parties, any party may file an answering brief 
which shall contain a subject index, with page references, and a table 
of cases (alphabetically arranged), textbooks, statutes, and other 
material cited, with page references thereto. Such brief shall present 
clearly the points of fact and law relied upon in support of the reasons 
the party has for each position urged, with specific page references to 
the record and legal or other materials relied upon.
    (d) Participant's brief. Within thirty (30) days after service of 
the appeal brief upon all parties, any participant may file a brief on 
appeal, presenting clearly the position urged.
    (e) Cross appeal. If a timely notice of appeal is filed by a party, 
any other party may file a notice of cross appeal within ten (10) days 
of the date on which the first notice of appeal was filed. Cross appeals 
shall be included in the answering brief and shall conform to the 
requirements for form, content, and filing specified in paragraph (b) of 
this section for an appeal brief. If an appeal is noticed but not 
perfected, no cross appeal shall be permitted and the notice of cross 
appeal shall be deemed void.

[[Page 92]]

    (f) Reply brief. A reply brief shall be limited to rebuttal of 
matters presented in answering briefs, including matters raised in 
cross-appeals. A reply brief shall be filed and served within fourteen 
(14) days after service of an answering brief, or on the day preceding 
the oral argument, whichever comes first.
    (g) Oral argument. The purpose of an oral argument is to emphasize 
and clarify the issues. The Commission may order oral argument upon 
request of any party or upon its own initiative. A transcript of oral 
arguments shall be prepared. A Commissioner absent from an oral argument 
may participate in the consideration of and decision on the appeal.



Sec. 1025.54  Review of initial decision in absence of appeal.

    The Commission may, by order, review a case not otherwise appealed 
by a party. Should the Commission so order, the parties shall, and 
participants may, file briefs in accordance with Sec. 1025.53, except 
that the Commission may, in its discretion, establish a different 
briefing schedule in its order. The Commission shall issue its order 
within forty (40) days after issuance of the Initial Decision. The order 
shall set forth the issues which the Commission will review and may make 
provision for the filing of briefs. If the filing of briefs is scheduled 
by the Commission, the order shall designate which party or parties 
shall file the initial brief and which party or parties may thereafter 
file an answering brief, or the order may designate the simultaneous 
filing of briefs by the parties.



Sec. 1025.55  Final decision on appeal or review.

    (a) Consideration of record. Upon appeal from or review of an 
Initial Decision, the Commission shall consider the record as a whole or 
such parts of the record as are cited or as may be necessary to resolve 
the issues presented and, in addition, shall, to the extent necessary or 
desirable, exercise all the powers which it could have exercised if it 
had made the Initial Decision.
    (b) Rendering of final decision. In rendering its decision, the 
Commission shall adopt, modify, or set aside the findings, conclusions, 
and order contained in the Initial Decision, and shall include in its 
Final Decision a statement of the reasons for its action and any 
concurring or dissenting opinions. The Commission shall issue an order 
reflecting its Final Decision.
    (c) Except as otherwise ordered by the Commission, the Commission 
shall endeavor to file its Decision within ninety (90) days after the 
filing of all briefs or after receipt of transcript of the oral 
argument, whichever is later.



Sec. 1025.56  Reconsideration.

    Within twenty (20) days after issuance of a Final Decision and Order 
by the Commission, any party may file a petition for reconsideration of 
such decision or order, setting forth the relief desired and the grounds 
in support of the petition. Any petition filed under this section must 
be confined to new questions raised by the decision or order upon which 
the petitioner had no previous opportunity to argue. Any party desiring 
to oppose such a petition shall file an opposition to the petition 
within ten (10) days after sevice of the petition. The filing of a 
petition for reconsideration shall not stay the effective date of the 
Final Decision and Order or toll the running of any statutory time 
period affecting the Decision or Order unless specifically ordered by 
the Commission.



Sec. 1025.57  Effective date of order.

    (a) Orders in proceedings arising under the Consumer Product Safety 
Act. An order of the Commission in proceedings arising under the 
Consumer Product Safety Act becomes effective upon receipt, unless 
otherwise ordered by the Commission.
    (b) Orders in proceedings arising under the Flammable Fabrics Act--
(1) Consent orders. An order in proceedings arising under the Flammable 
Fabrics Act, which has been issued following the Commission's acceptance 
of an offer of settlement in accordance with Sec. 1025.26 of these 
rules, becomes effective upon receipt of notice of Commission 
acceptance, unless otherwise ordered by the Commission.

[[Page 93]]

    (2) Litigated orders. All other orders in proceedings arising under 
the Flammable Fabrics Act become effective upon the expiration of the 
statutory period for court review specified in Section 5(c) of the 
Federal Trade Commission Act, title 15, United States Code, section 
45(c), or, if a petition for review has been filed, upon a court's 
affirmance of the Commission's order.
    (c) Consequences of failure to comply with effective order. A 
respondent against whom an order has been issued who is not in 
compliance with such order on or after the date the order becomes 
effective is in violation of such order and is subject to an immediate 
action for the civil or criminal penalties provided for in the 
applicable statute.



Sec. 1025.58  Reopening of proceedings.

    (a) General. Any proceedings may be reopened by the Commission at 
any time, either on its own initiative or upon petition of any party to 
the proceedings.
    (b) Exception. Proceedings arising under the Flammable Fabrics Act 
shall not be reopened while pending in a United States court of appeals 
on a petition for review after the transcript of the record has been 
filed, or while pending in the Supreme Court of the United States.
    (c) Commission-originated reopening--(1) Before effective date of 
order. At any time before the effective date of a Commission order, the 
Commission may, upon its own initiative and without prior notice to the 
parties, reopen any proceedings and enter a new decision or order to 
modify or set aside, in whole or in part, the decision or order 
previously issued.
    (2) After effective date of order. Whenever the Commission is of the 
opinion that changed conditions of fact or law or the public interest 
may require that a Commission decision or order be altered, modified, or 
set aside in whole or in part, the Commission shall serve upon all 
parties to the original proceedings an order to show cause, stating the 
changes the Commission proposes to make in the decision or order and the 
reasons such changes are deemed necessary. Within thirty (30) days after 
service of an order to show cause, any party to the original 
proceedings, may file a response. Any party not responding to the order 
to show cause within the time allowed shall be considered to have 
consented to the proposed changes.
    (d) Petition for reopening. Whenever any person subject to a final 
order is of the opinion that changed conditions of fact or law require 
that the decision or order be altered, modified, or set aside, or that 
the public interest so requires, that person may petition the Commission 
to reopen the proceedings. The petition shall state the changes desired 
and the reasons those changes should be made, and shall include such 
supporting evidence and argument as will, in the absence of any 
opposition, provide the basis for a Commission decision on the petition. 
The petition shall be served upon all parties to the original 
proceedings. Within thirty (30) days after service of the petition, 
Complaint Counsel shall file a response. Any other party to the original 
proceedings also may file a response within that period.
    (e) Hearings--(1) Unopposed. Where an order to show cause or 
petition to reopen is not opposed, or is opposed but the pleadings do 
not raise issues of fact to be resolved, the Commission, in its 
discretion, may decide the matter on the order to show cause or petition 
and responses, or it may serve upon the parties a notice of hearing 
containing the date when the matter will be heard. The proceedings 
normally will be limited to the filing of briefs but may include oral 
argument when deemed necessary by the Commission.
    (2) Factual issues. When the pleadings raise substantial factual 
issues, the Commission may direct such hearings as it deems appropriate. 
Upon conclusion of the hearings, and after opportunity for the parties 
to file post-hearing briefs containing proposed findings of fact and 
conclusions of law, as well as a proposed order, the Presiding Officer 
shall issue a Recommended Decision, including proposed findings and 
conclusions, and the reasons, as well as a proposed Commission order. If 
the Presiding Officer recommends that the Commission's original order be 
reopened, the proposed order shall include appropriate provisions for 
the alteration, modification or setting aside

[[Page 94]]

of the original order. The record and the Presiding Officer's 
Recommended Decision shall be certified to the Commission for final 
disposition of the matter.
    (f) Commission disposition. Where the Commission has ordered a 
hearing, upon receipt of the Presiding Officer's Recommended Decision, 
the Commission shall make a decision and issue an order based on the 
hearing record as a whole. If the Commission determines that changed 
conditions of fact or law or the public interest requires, it shall 
reopen the order previously issued; alter, modify, or set aside the 
order's provisions in whole or in part; and issue an amended order 
reflecting the alterations, modifications, or deletions. If the 
Commission determines that the original order should not be reopened, it 
shall issue an order affirming the original order. A decision stating 
the reasons for the Commission's order shall accompany the order.



              Subpart G--Appearances, Standards of Conduct



Sec. 1025.61  Who may make appearances.

    A party or participant may appear in person, or by a duly authorized 
officer, partner, regular employee, or other agent of the party or 
participant, or by counsel or other duly qualified representative, in 
accordance with Sec. 1025.65.



Sec. 1025.62  Authority for representation.

    Any individual acting in a representative capacity in any 
adjudicative proceedings may be required by the Presiding Officer or the 
Commission to show his/her authority to act in such capacity. A regular 
employee of a party who appears on behalf of the party may be required 
by the Presiding Officer or the Commission to show his/her authority to 
so appear.



Sec. 1025.63  Written appearances.

    (a) Filing. Any person who appears in any proceedings shall file a 
written notice of appearance with the Secretary or deliver a written 
notice of appearance to the Presiding Officer at the hearing, stating 
for whom the appearance is made and the name, address, and telephone 
number (including area code) of the person making the appearance and the 
date of the commencement of the appearance. The written appearance shall 
be made a part of the record.
    (b) Withdrawal. Any person who has previously appeared in any 
proceedings may withdraw his/her appearance by filing a written notice 
of withdrawal of appearance with the Secretary. The notice of withdrawal 
of appearance shall state the name, address, and telephone number 
(including area code) of the person withdrawing the appearance, for whom 
the appearance was made, and the effective date of the withdrawal of the 
appearance. Such notice of withdrawal shall be filed within five (5) 
days of the effective date of the withdrawal of the appearance.



Sec. 1025.64  Attorneys.

    Any attorney at law who is admitted to practice before any United 
States court or before the highest court of any State, the District of 
Columbia, or any territory or commonwealth of the United States, may 
practice before the Commission. An attorney's own representation that 
he/she is in good standing before any of such courts shall be sufficient 
proof thereof, unless otherwise directed by the Presiding Officer or the 
Commission.



Sec. 1025.65  Persons not attorneys.

    (a) Filing and approval of proof of qualifications. Any person who 
is not an attorney at law may be admitted to appear in any adjudicative 
proceedings as a representative of any party or participant if that 
person files proof to the satisfaction of the Presiding Officer that he/
she possesses the necessary knowledge of administrative procedures, 
technical, or other qualifications to render valuable service in the 
proceedings and is otherwise competent to advise and assist in the 
presentation of matters in the proceedings. An application by a person 
not an attorney at law for admission to appear in any proceedings shall 
be submitted in writing to the Secretary, not later than thirty (30) 
days prior to the hearing. The application shall set forth in detail the 
applicant's qualifications to appear in the proceedings.

[[Page 95]]

    (b) Exception. Any person who is not an attorney at law and whose 
application has not been approved shall not be permitted to appear in 
Commission proceedings. However, this provision shall not apply to any 
person who appears before the Commission on his/her own behalf or on 
behalf of any corporation, partnership, or unincorporated association of 
which the person is a partner or general officer.



Sec. 1025.66  Qualifications and standards of conduct.

    (a) Good faith transactions. The Commission expects all persons 
appearing in proceedings before the Commission or the Presiding Officer 
to act with integrity, with respect, and in an ethical manner. Business 
transacted before and with the Commission or the Presiding Officer shall 
be conducted in good faith.
    (b) Exclusion of parties, participants, or their representatives. To 
maintain orderly proceedings, the Commission or the Presiding Officer 
may exclude parties, participants, or their representatives for refusal 
to comply with directions, continued use of dilatory tactics, refusal to 
adhere to reasonable standards of orderly and ethical conduct, failure 
to act in good faith, or violation of the prohibition in Sec. 1025.68 
against certain ex parte communications.
    (c) Exclusions from the record. The Presiding Officer or the 
Commission may disregard and order the exclusion from the record of any 
written or oral submissions or representations which are not made in 
good faith or which are unfair, incomplete, or inaccurate.
    (d) Appeal by excluded party. An excluded party, participant, or 
representative may petition the Commission to entertain an interlocutory 
appeal in accordance with Sec. 1025.24 of these rules. If, after such 
appeal, the representative of a party or participant is excluded, the 
hearing shall, at the request of the party or participant, be suspended 
for a reasonable time so that the party or participant may obtain 
another representative.



Sec. 1025.67  Restrictions as to former members and employees.

    (a) Generally. Except as otherwise provided in paragraph (b) of this 
section, the post-employee restrictions applicable to former Commission 
members and employees, as set forth in the Commission's ``Post 
Employment Restrictions Applicable to Former Commission Officers and 
Employees'', 16 CFR part 1030, subpart L, shall govern the activities of 
former Commission members and employees in matters connected with their 
former duties and responsibilities.
    (b) Participation as witness. A former member or employee of the 
Commission may testify in any proceeding subject to these Rules 
concerning his/her participation in any Commission activity. This 
section does not constitute a waiver by the Commission of any objection 
provided by law to testimony that would disclose privileged or 
confidential material. The provisions of 18 U.S.C. 1905 prohibiting the 
disclosure of trade secrets also applies to testimony by former members 
and employees.
    (c) Procedure for requesting authorization to appear. In cases to 
which paragraph (a) of this section is applicable, a former member or 
employee of the Commission may request authorization to appear or 
participate in any proceedings or investigation by filing with the 
Secretary a written application disclosing the following information:
    (1) The nature and extent of the former member's or employee's 
participation in, knowledge of, and connection with the proceedings or 
investigation during his/her service with the Commission;
    (2) Whether the files of the proceedings or investigation came to 
his/her attention;
    (3) Whether he/she was employed in the directorate, division, or 
other organizational unit within the Commission in which the proceedings 
or investigation is or has been pending;
    (4) Whether he/she worked directly or in close association with 
Commission personnel assigned to the proceedings or investigation and, 
if so, with whom and in what capacity; and
    (5) Whether during service with the Commission, he/she was engaged 
in any matter concerning the person involved in the proceedings or 
investigation.
    (d) Denial of request to appear. The requested authorization shall 
not be given in any case:

[[Page 96]]

    (1) Where it appears that the former member or employee, during 
service with the Commission, participated personally and substantially 
in the proceedings or investigation; or
    (2) Where the Commission is not satisfied that the appearance or 
participation will not involve any actual or apparent impropriety; or
    (3) In any case which would result in a violation of title 18, 
United States Code, section 207.



Sec. 1025.68  Prohibited communications.

    (a) Applicability. This section is applicable during the period 
commencing with the date of issuance of a complaint and ending upon 
final Commission action in the matter.
    (b) Definitions--(1) Decision-maker. Those Commission personnel who 
render decisions in adjudicative proceedings under these rules, or who 
advise officials who render such decisions, including:
    (i) The Commissioners and their staffs;
    (ii) The Administrative Law Judges and their staffs;
    (iii) The General Counsel and his/her staff, unless otherwise 
designated by the General Counsel.
    (2) Ex parte communication. (i) Any written communication concerning 
a matter in adjudication which is made to a decision-maker by any person 
subject to these Rules, which is not served on all parties; or
    (ii) Any oral communication concerning a matter in adjudication 
which is made to a decision-maker by any person subject to these Rules, 
without advance notice to all parties to the proceedings and opportunity 
for them to be present.
    (c) Prohibited ex parte communications. Any oral or written ex parte 
communication relative to the merits of any proceedings under these 
Rules is a prohibited ex parte communication, except as otherwise 
provided in paragraph (d) of this section.
    (d) Permissible ex parte communications. The following 
communications shall not be prohibited under this section.
    (1) Ex parte communications authorized by statute or by these rules. 
(See, for example, Sec. 1025.38 which governs applications for the 
issuance of subpoenas.)
    (2) Any staff communication concerning judicial review or judicial 
enforcement in any matter pending before or decided by the Commission.
    (e) Procedures for handling prohibited ex parte communication--(1) 
Prohibited written ex parte communication. To the extent possible, a 
prohibited written ex parte communication received by any Commission 
employee shall be forwarded to the Secretary rather than to a decision-
maker. A prohibited written ex parte communication which reaches a 
decision-maker shall be forwarded by the decision-maker to the 
Secretary. If the circumstances in which a prohibited ex parte written 
communication was made are not apparent from the communication itself, a 
statement describing those circumstances shall be forwarded with the 
communication.
    (2) Prohibited oral ex parte communication. (i) If a prohibited oral 
ex parte communication is made to a decision-maker, he/she shall advise 
the person making the communication that the communication is prohibited 
and shall terminate the discussion; and
    (ii) In the event of a prohibited oral ex parte communication, the 
decision-maker shall forward to the Secretary a signed and dated 
statement containing such of the following information as is known to 
him/her.
    (A) The title and docket number of the proceedings;
    (B) The name and address of the person making the communication and 
his/her relationship (if any) to the parties and/or participants to the 
proceedings;
    (C) The date and time of the communication, its duration, and the 
circumstances (e.g., telephone call, personal interview, etc.) under 
which it was made;
    (D) A brief statement of the substance of the matters discussed; and
    (E) Whether the person making the communication persisted in doing 
so after being advised that the communication was prohibited.
    (3) Filing. All communications and statements forwarded to the 
Secretary under this section shall be placed in a public file which 
shall be associated with, but not made a part of, the

[[Page 97]]

record of the proceedings to which the communication or statement 
pertains.
    (4) Service on parties. The Secretary shall serve a copy of each 
communication and statement forwarded under this section on all parties 
to the proceedings. However, if the parties are numerous, or if other 
circumstances satisfy the Secretary that service of the communication or 
statement would be unduly burdensome, he/she, in lieu of service, may 
notify all parties in writing that the communication or statement has 
been made and filed and that it is available for insection and copying.
    (5) Service on maker. The Secretary shall forward to the person who 
made the prohibited ex parte communication a copy of each communication 
or statement filed under this section.
    (f) Effect of ex parte communications. No prohibited ex parte 
communication shall be considered as part of the record for decision 
unless introduced into evidence by a party to the proceedings.
    (g) Sanctions. A person subject to these Rules who make, a 
prohibited ex parte communication, or who encourages or solicits another 
to make any such communication, may be subject to any appropriate 
sanction or sanctions, including but not limited to, exclusion from the 
proceedings and an adverse ruling on the issue which is the subject of 
the prohibited communication.



    Subpart H--Implementation of the Equal Access to Justice Act in 
              Adjudicative Proceedings With the Commission

    Authority: Equal Access to Justice Act, Pub. L. 96-481, 94 Stat. 
2325, 5 U.S.C. 504 and the Administrative Procedure Act, 5 U.S.C. 551 et 
seq.

    Source: 47 FR 25513, June 14, 1982, unless otherwise noted.



Sec. 1025.70  General provisions.

    (a) Purpose of this rule. The Equal Access to Justice Act, 5 U.S.C. 
504 (called ``the EAJA'' in this subpart), provides for the award of 
attorney fees and other expenses to eligible persons who are parties to 
certain adversary adjudicative proceedings before the Commission. An 
eligible party may receive an award when it prevails over Commission 
complaint counsel, unless complaint counsel's position in the proceeding 
was substantially justified or special circumstances make an award 
unjust. This subpart describes the parties eligible for awards and the 
proceedings covered. The rules also explain how to apply for awards and 
the procedures and standards that the Commission will use to make them.
    (b) When the EAJA applies. The EAJA applies to any adversary 
adjudicative proceeding pending before the Commission at any time 
between October 1, 1981 and September 30, 1984. This includes 
proceedings commenced before October 1, 1981, if final Commission action 
has not been taken before that date, and proceedings pending on 
September 30, 1984, regardless of when they were initiated or when final 
Commission action occurs.
    (c) Proceedings covered. (1) The EAJA and this rule apply to 
adversary adjudicative proceedings conducted by the Commission. These 
are adjudications under 5 U.S.C. 554 in which the position of the 
Commission or any component of the Commission is represented by an 
attorney or other representative who enters an appearance and 
participates in the proceeding. The rules in this subpart govern 
adversary adjudicative proceedings relating to the provisions of 
sections 15 (c), (d) and (f) and 17(b) of the Consumer Product Safety 
Act (15 U.S.C. 2064 (c) (d) and (f); 2066(b)), sections 3 and 8(b) of 
the Flammable Fabrics Act (15 U.S.C. 1192, 1197(b)), and section 15 of 
the Federal Hazardous Substances Act (15 U.S.C. 1274), which are 
required by statute to be determined on the record after opportunity for 
a public hearing. These rules will also govern administrative 
adjudicative proceedings for the assessment of civil penalties under 
section 20(a) of the Consumer Product Safety Act (15 U.S.C. 2068(a)). 
See 16 CFR 1025.1.
    (2) The Commission may designate a proceeding not listed in 
paragraph (c)(1) of this section as an adversary adjudicative proceeding 
for purposes of the EAJA by so stating in an order initiating the 
proceeding or designating

[[Page 98]]

the matter for hearing. The Commission's failure to designate a 
proceeding as an adversary adjudicative proceeding shall not preclude 
the filing of an application by a party who believes the proceeding is 
covered by the EAJA. Whether the proceeding is covered will then be an 
issue for resolution in proceedings on the application.
    (3) If a proceeding includes both matters covered by the EAJA and 
matters specifically excluded from coverage, any award made will include 
only fees and expenses related to covered issues.
    (d) Eligibility of applicants. (1) To be eligible for an award of 
attorney fees and other expenses under the EAJA, the applicant must be a 
party to the adversary adjudication for which it seeks an award. The 
term ``party'' is defined in 5 U.S.C. 551(3) and 16 CFR 1025.3(f). The 
applicant must show that it meets all conditions of eligibility set out 
in this paragraph and in Sec. 1025.71.
    (2) The types of eligible applicants are:
    (i) Individuals with a net worth of not more than $1 million;
    (ii) Sole owners of unincorporated businesses who have a net worth 
of not more than $5 million including both personal and business 
interests, and not more than 500 employees;
    (iii) Charitable or other tax-exempt organizations described in 
section 501(c)(3) of the Internal Revenue Code (26 U.S.C. 501(c)(3)) 
which have not more than 500 employees;
    (iv) Any other partnership, corporation, association, or public or 
private organization with a net worth of not more than $5 million and 
which have not more than 500 employees.
    (3) For the purpose of eligibility, the net worth and number of 
employees of an applicant shall be determined as of the date the 
proceeding was initiated.
    (4) An applicant who owns an unincorporated business will be 
considered as an ``individual'' rather than as a ``sole owner of an 
unincorporated business'' if the issues on which the applicant prevails 
are related primarily to personal interests rather than to business 
interests.
    (5) The number of employees of an applicant include all persons who 
regularly perform services for remuneration for the applicant, under the 
applicant's direction and control. Part-time employees shall be included 
on a proportional basis.
    (6) The net worth and number of employees of the applicant and all 
of its affiliates shall be aggregated to determine eligibility. For this 
purpose, affiliate means (i) An individual, corporation or other entity 
that directly or indirectly controls or owns a majority of the voting 
shares or other interest of the applicant, or (ii) Any corporation or 
other entity of which the applicant directly or indirectly owns or 
controls a majority of the voting shares or other interest. However, the 
presiding officer may determine that such treatment would be unjust and 
contrary to the purposes of the EAJA in light of the actual relationship 
between the affiliated entities. In addition, the presiding officer may 
determine that financial relationships of the applicant other than those 
described in this paragraph constitute special circumstances that would 
make an award unjust.
    (7) An applicant that participates in a proceeding primarily on 
behalf of one or more other persons or entities that would be ineligible 
is not itself eligible for an award.
    (8) An applicant that represents himself/herself regardless of 
whether he is licensed to practice law may be awarded all such expenses 
and fees available to other prevailing eligible parties. See 16 CFR 
1025.61 and 1025.65 of the Commission's rules.
    (e) Standards for awards. (1) An eligible prevailing applicant may 
receive an award for fees and expenses incurred in connection with a 
proceeding, or in a significant and discrete substantive portion of the 
proceeding, unless the position of Commission complaint counsel over 
which the applicant has prevailed was substantially justified. Complaint 
counsel bear the burden of proof that an award should not be made to an 
eligible prevailing applicant. Complaint counsel may avoid the granting 
of an award by showing that its position was reasonable in law and fact.
    (2) An award will be reduced or denied if the applicant has unduly 
or unreasonably protracted the proceeding or if special circumstances 
make the award sought unjust.

[[Page 99]]

    (f) Allowable fees and expenses. (1) Awards will be based on rates 
customarily charged by persons engaged in the business of acting as 
attorneys, agents and expert witnesses, even if the services were made 
available without charge or at a reduced rate to the applicant.
    (2) No award for the fee of an attorney or agent under these rules 
may exceed $75 per hour. No award to compensate an expert witness may 
exceed the highest rate at which the Commission is authorized to pay 
expert witnesses. However, an award may also include the reasonable 
expenses of the attorney, agent, or witness as a separate item, if the 
attorney, agent or witness ordinarily charges clients separately for 
such expenses.
    (3) In determining the reasonableness of the fee sought for an 
attorney, agent or expert witness, the presiding officer shall consider 
the following:
    (i) If the attorney, agent or witness is in private practice, his or 
her customary fee for similar services, or, if an employee of the 
applicant, the fully allocated cost of the services;
    (ii) The prevailing rate for similar services in the community in 
which the attorney, agent or witness ordinarily performs services;
    (iii) The time actually spent in the representation of the 
applicant;
    (iv) The time reasonably spent in light of the difficulty or 
complexity of the issues in the proceeding; and
    (v) Such other factors as may bear on the value of the services 
provided.
    (4) The reasonable cost of any study, analysis, engineering report, 
test, project or similar matter prepared on behalf of a party may be 
awarded, to the extent that the charge for the service does not exceed 
the prevailing rate for similar services, and the study or other matter 
was necessary for preparation of the applicant's case.
    (5) Fees may be awarded to eligible applicants only for service 
performed after the issuance of a complaint and the commencement of the 
adjudicative proceeding in accordance with 16 CFR 1025.11(a).
    (g) Rulemaking on maximum rates for attorney fees. (1) If warranted 
by an increase in the cost of living or by special circumstances, the 
Commission may adopt regulations providing that attorney fees may be 
awarded at a rate higher than $75 per hour in some or all of the types 
of proceedings covered by this subpart. The Commission will conduct any 
rulemaking proceedings for this purpose under the informal rulemaking 
procedures of the Administrative Procedure Act, 5 U.S.C. 533.
    (2) Any person may file with the Commission a petition for 
rulemaking to increase the maximum rate for attorney fees, in accordance 
with the Administrative Procedure Act, 5 U.S.C. 553(e). The petition 
should identify the rate the petitioner believes the Commission should 
establish and the types of proceedings in which the rate should be used. 
The petition should also explain fully the reasons why the higher rate 
is warranted. The Commission will respond to the petition within a 
reasonable time after it is filed, by initiating a rulemaking 
proceeding, denying the petition, or taking other appropriate action.
    (h) Presiding officer. The presiding oficer in a proceeding covered 
by this regulation is a person as defined in the Commission's Rules, 16 
CFR 1025.3(i), who conducts an adversary adjudicative proceeding.



Sec. 1025.71  Information required from applicant.

    (a) Contents of application. (1) An application for an award of fees 
and expenses under the EAJA shall identify the applicant and the 
proceeding for which an award is sought. The application shall show that 
the applicant has prevailed and identify the position of complaint 
counsel in the adjudicative proceeding that the applicant alleges was 
not substantially justified. Unless the applicant is an individual, the 
application shall also state the number of employees of the applicant 
and describe briefly the type and purpose of its organization or 
business.
    (2) The application shall also include a verified statement that the 
applicant's net worth does not exceed $1 million (if an individual) or 
$5 million (for all other applicants, including their affiliates). 
However, an applicant may omit this statement if it attaches

[[Page 100]]

a copy of a ruling by the Internal Revenue Service that it qualifies as 
an organization described in section 501(c)(3) of the Internal Revenue 
Code or, in the case of a tax-exempt organization not required to obtain 
a ruling from the Internal Revenue Service on its exempt status, a 
statement that describes the basis for the applicant's belief that it 
qualifies under such section.
    (3) The application shall state the amount of fees and expenses for 
which an award is sought.
    (4) The application may also include any other matters that the 
applicant wishes the Commission to consider in determining whether and 
in what amount an award should be made.
    (5) The application shall be signed by the applicant or an 
authorized officer or attorney of the applicant. It shall also contain 
or be accompanied by a written verification under oath or under penalty 
of perjury that the information provided in the application is true and 
correct.
    (b) Net worth exhibit; confidential treatment. (1) Each applicant 
except a qualified tax-exempt organization or cooperative association 
must provide with its application a detailed exhibit showing the net 
worth of the applicant and any affiliates (as defined in 
Sec. 1025.70(d)(6) of this subpart) when the proceeding was initiated. 
The exhibit may be in any form convenient to the applicant that provides 
full disclosure of the applicant's and its affiliates' assets and 
liabilities and is sufficient to determine whether the applicant 
qualifies under the standards in this subpart. The presiding officer may 
require an applicant to file additional information to determine its 
eligibility for an award.
    (2) Ordinarily, the net worth exhibit will be included in the public 
record of the proceeding. However, an applicant that objects to public 
disclosure of information in any portion of the exhibit or to public 
disclosure of any other information submitted, and believes there are 
legal grounds for withholding it from disclosure, may move to have that 
information kept confidential and excluded from public disclosure in 
accordance with Sec. 1025.45 of the Commission rules for in camera 
materials, 16 CFR 1025.45. This motion shall describe the information 
sought to be withheld and explain, in detail, why it falls within one or 
more of the specific exemptions from mandatory disclosure under the 
Freedom of Information Act, 5 U.S.C. 552(b)(1)-(9).
    (3) Section 6(a)(2) of the Consumer Product Safety Act, 15 U.S.C. 
2055(a)(2), provides that certain information which contains or relates 
to a trade secret or other matter referred to in section 1905 of title 
18, United States Code, or subject to 5 U.S.C. 552(b)(4) shall not be 
disclosed. This prohibition is an Exemption 3 statute under the Freedom 
of Information Act, 5 U.S.C. 552(b)(3). Material submitted as part of an 
application for which in camera treatment is granted shall be available 
to other parties only in accordance with 16 CFR 1025.45(c) of the 
Commission Rules and, if applicable, section 6(a)(2) of the CPSA. If the 
presiding officer determines that the information should not be withheld 
from disclosure because it does not fall within section 6(a)(2) of the 
CPSA, he shall place the information in the public record but only after 
notifying the submitter of the information in writing of the intention 
to disclose such document at a date not less than 10 days after the date 
of receipt of notification. Otherwise, any request to inspect or copy 
the exhibit shall be disposed of in accordance with the Commission's 
established procedures under the Freedom of Information Act (see 16 CFR 
part 1015).
    (c) Documentation of fees and expenses. The application shall be 
accompanied by full documentation of the fees and expenses, including 
the cost of any study, analysis, engineering report, test, project or 
similar matter, for which an award is sought. A separate itemized 
statement shall be submitted for each professional firm or individual 
whose services are covered by the application, showing the hours spent 
in connection with the proceeding by each individual, a description of 
the specific services performed, the rate at which each fee has been 
computed, any expenses for which reimbursement is sought, the total 
amount claimed, and the total amount paid or payable by the applicant or 
by any other person or entity for the services provided. The presiding 
officer may require the applicant to provide vouchers, receipts; or

[[Page 101]]

other substantiation for any expenses claimed.
    (d) When an application may be filed. (1) An application may be 
filed whenever the applicant has prevailed in a proceeding covered by 
this subpart or in a significant and discrete substantive portion of the 
proceeding. However, an application must be filed no later than 30 days 
after the Commission's final disposition of such a proceeding.
    (2) If review or reconsideration is sought or taken of a decision as 
to which an applicant believes it has prevailed, proceedings for the 
award of fees shall be stayed pending final disposition of the 
underlying controversy.
    (3) If review or reconsideration is sought or taken of a decision as 
to which an applicant believes it has prevailed, proceedings for the 
award of fees shall be stayed pending final disposition of the 
underlying controversy.
    (4) For purposes of this subpart, final disposition means the later 
of:
    (i) The date on which an initial decision by the presiding officer 
becomes final, see 16 CFR 1025.52;
    (ii) The date on which the Commission issues a final decision (See 
16 CFR 1025.55);
    (iii) The date on which the Commission issues an order disposing of 
any petitions for reconsideration of the Commission's final order in the 
proceeding (See 16 CFR 1025.56; or
    (iv) Issuance of a final order or any other final resolution of a 
proceeding, such as a settlement or voluntary dismissal, which is not 
subject to a petition for reconsideration.
    (e) Where an application must be filed. The application for award 
and expenses must be submitted to the Office of the Secretary, Consumer 
Product Safety Commission, Washington, D.C. 20207 in accordance with the 
application requirements of this section.



Sec. 1025.72  Procedures for considering applications.

    (a) Filing and service of documents. Any application for an award or 
other pleading or document related to an application shall be filed and 
served on all parties to the proceeding in the same manner as provided 
in the Commission's Rules of Practice, 16 CFR 1025.11-1025.19.
    (b) Answer to application. (1) Within 30 days after service of an 
application for an award of fees and expenses, complaint counsel in the 
underlying administrative proceeding upon which the application is based 
may file an answer to the application. Unless complaint counsel requests 
an extension of time for filing or files a statement of intent to 
negotiate under paragraph (b)(2) of this section, failure to file an 
answer within the 30-day period may be treated as a consent to the award 
requested.
    (2) If complaint counsel and the applicant believe that the issues 
in the fee application can be settled, they may jointly file a statement 
of their intent to negotiate a settlement. The filing of this statement 
shall extend the time for filing an answer for an additional 30 days, 
and further extensions may be granted by the presiding officer upon 
request by complaint counsel and the applicant.
    (3) The answer shall explain in detail any objections to the award 
requested and identify the facts relied on in support of Commission 
counsel's position. If the answer is based on any alleged facts not 
already in the record of the proceeding, complaint counsel shall include 
with the answer either supporting affidavits or a request for further 
proceedings under paragraph (f) of this section.
    (c) Reply. Within 15 days after service of an answer, the applicant 
may file a reply. If the reply is based on any alleged facts not already 
in the record of the proceeding, the applicant shall include with the 
reply either supporting affidavits or a request for further proceedings 
under paragraph (f) of this section.
    (d) Comments by other parties. Any party to a proceeding other than 
the applicant and complaint counsel may file comments on an application 
within 30 days after it is served or on an answer within 15 days after 
it is served. A commenting party may not participate further in 
proceedings on the application unless the presiding officer determines 
that the public interest requires such participation in order to permit

[[Page 102]]

full exploration of matters raised in the comments.
    (e) Settlement. The applicant and complaint counsel may agree on a 
proposed settlement of the award before final action on the application, 
either in connection with a settlement of the underlying proceeding, or 
after the underlying proceeding has been concluded, in accordance with 
the Commission's standard settlement procedure (See 16 CFR 1115.20(b), 
1118.20, 1025.26, and 1605.3). If a prevailing party and complaint 
counsel agree on a proposed settlement of an award before an application 
has been filed, the application shall be filed with the proposed 
settlement.
    (f) Further proceedings. (1) Ordinarily, the determination of an 
award will be made on the basis of the written record. However, on 
request of either the applicant or complaint counsel, or on his or her 
own initiative, the presiding officer may order further proceedings. 
Such further proceedings shall be held only when necessary for full and 
fair resolution of the issues arising from the application, and shall be 
conducted as promptly as possible.
    (2) A request that the presiding officer order further proceedings 
under this paragraph shall specifically identify the information sought 
or the disputed issues and shall explain why the additional proceedings 
are necessary to resolve the issues.
    (g) Initial decision. The presiding officer shall endeavor to issue 
an initial decision on the application within 30 days after completion 
of proceedings on the application. The decision shall include written 
findings and conclusions on the applicant's eligibility and status as a 
prevailing party, and an explanation of the reasons for any difference 
between the amount requested and the amount awarded. The decision shall 
also include, if at issue, findings on whether the complaint counsel's 
position was substantially justified, whether the applicant unduly 
protracted the proceedings, or whether special circumstances make an 
award unjust. If the applicant has sought an award against more than one 
agency, the decision of this Commission will only address the allocable 
portion for which this Commission is responsible to the eligible 
prevailing party.
    (h) Agency review. (1) Either the applicant or complaint counsel may 
seek review of the initial decision on the fee application, or the 
Commission may decide to review the decision on its own initiative, in 
accordance with 16 CFR 1025.54, 1025.55 and 1025.56.
    (2) If neither the applicant nor Commission complaint counsel seeks 
review and the Commission does not take review on its own initiative, 
the initial decision on the application shall become a final decision of 
the Commission 30 days after it is issued.
    (3) If an appeal from or review of an initial decision under this 
subpart is taken, the Commission shall endeavor to issue a decision on 
the application within 90 days after the filing of all briefs or after 
receipt of transcripts of the oral argument, whichever is later, or 
remand the application to the presiding officer for further proceedings.
    (i) Judicial review. Judicial review of final Commission decisions 
on awards may be sought as provided in 5 U.S.C. 504(c)(2).
    (j) Payment of award. An applicant seeking payment of an award shall 
submit to the Secretary of the Commission a copy of the Commission's 
final decision granting the award, accompanied by a verified statement 
that the applicant will not seek review of the decision in the United 
States courts. (Office of the Secretary, Consumer Product Safety 
Commission, Washington, D.C. 20207.) The Commission will pay the amount 
awarded to the applicant within 60 days, unless judicial review of the 
award or of the underlying decision of the adversary adjudication has 
been sought by the applicant or any other party to the proceeding. 
Comments and accompanying material may be seen in or copies obtained 
from the Office of the Secretary, Consumer Product Safety Commission, 
Washington, D.C. 20207, during working hours Monday through Friday.

    Appendix I to Part 1025--Suggested Form of Final Prehearing Order

                              Case Caption

    A final prehearing conference was held in this matter, pursuant to 
Rule 21 of the Commission's Rules of Practice for Adjudicative

[[Page 103]]

Proceedings (16 CFR 1025.21), on the ------ day of ------------, 19--, 
at ---- o'clock, -- stm.
    Counsel appeared as follows:
    For the Commission staff:
    For the Respondent(s):
    Others:
    1. Nature of Action and Jurisdiction. This is an action for --------
------------ and the jurisdiction of the Commission is invoked under 
United States Code, Title------------, Section ------------ and under 
the Code of Federal Regulations, Title --------, Section --------. The 
jurisdiction of the Commission is (not) disputed. The question of 
jurisdiction was decided as follows:
    2. Stipulations and Statements. The following stipulation(s) and 
statement(s) were submitted, attached to, and made a part of this order:
    (a) A comprehensive written stipulation or statement of all 
uncontested facts;
    (b) A concise summary of the ultimate facts as claimed by each 
party. (Complaint Counsel must set forth the claimed facts, 
specifically; for example, if a violation is claimed, Complaint Counsel 
must assert specifically the acts of violation complained of; each 
respondent must reply with equal clarity and detail.)
    (c) Written stipulation(s) or statement(s) setting forth the 
qualifications of the expert witnesses to be called by each party;
    (d) Written list(s) of the witnesses whom each party will call, 
written list(s) of the additional witnesses whom each party may call, 
and a statement of the subject matter on which each witness will 
testify;
    (e) An agreed statement of the contested issues of fact and of law, 
or separate statements by each party of any contested issues of fact and 
law not agreed to;
    (f) A list of all depositions to be read into evidence and 
statements of any objections thereto;
    (g) A list and brief description of any charts, graphs, models, 
schematic diagrams, and similar objects that will be used in opening 
statements or closing arguments but will not be offered in evidence. If 
any other such objects are to be used by any party, those objects will 
be submitted to opposing counsel at least three days prior to the 
hearing. If there is then any objection to their use, the dispute will 
be submitted to the Presiding Officer at least one day prior to the 
hearing;
    (h) Written waivers of claims or defenses which have been abandoned 
by the parties.
    The foregoing were modified at the pretrial conference as follows:
(To be completed at the conference itself. If none, recite ``none''.)
    3. Complaint Counsel's Evidence. 3.1 The following exhibits were 
offered by Complaint Counsel, received in evidence, and marked as 
follows:
(Identification number and brief description of each exhibit)
    The authenticity of these exhibits has been stipulated.
    3.2 The following exhibits were offered by Complaint Counsel and 
marked for identification. There was reserved to the respondent(s) (and 
party intervenors) the right to object to their receipt in evidence on 
the grounds stated:
(Identification number and brief description of each exhibit. State 
briefly ground of objection, e.g., competency, relevancy, materiality)
    4. Respondent's Evidence. 4.1 The following exhibits were offered by 
the respondent(s), received in evidence, and marked as herein indicated:
(Identification number and brief description of each exhibit)
    The authenticity of these exhibits has been stipulated.
    4.2 The following exhibits were offered by the respondent(s) and 
marked for identification. There was reserved to Complaint Counsel (and 
party intervenors) the right to object to their receipt in evidence on 
the grounds stated:
(Identification number and brief description of each exhibit. State 
briefly ground of objection, e.g., competency, relevancy, materiality)
    5. Party Intervenor's Evidence. 5.1 The following exhibits were 
offered by the party intervenor(s), received in evidence, and marked as 
herein indicated:
(Identification number and brief description of each exhibit)
    The authenticity of these exhibits has been stipulated.
    5.2 The following exhibits were offered by the party intervenor(s) 
and marked for identification. There was reserved to Complaint Counsel 
and respondent(s) the right to object to their receipt in evidence on 
the grounds stated:
(Identification number and brief description of each exhibit. State 
briefly ground of objection, e.g., competency, relevancy, materiality)

    Note: If any other exhibits are to be offered by any party, such 
exhibits will be submitted to opposing counsel at least ten (10) days 
prior to hearing, and a supplemental note of evidence filed into this 
record.

    6. Additional Actions. The following additional action(s) were 
taken:
(Amendments to pleadings, agreements of the parties, disposition of 
motions, separation of issues of liability and remedy, etc., if 
necessary)
    7. Limitations and Reservations. 7.1 Each of the parties has the 
right to further supplement the list of witnesses not later than ten 
(10) days prior to commencement of the hearing by furnishing opposing 
counsel with the

[[Page 104]]

name and address of the witness and general subject matter of his/her 
testimony and by filing a supplement to this pretrial order. Thereafter, 
additional witnesses may be added only after application to the 
Presiding Officer, for good cause shown.
    7.2 Rebuttal witnesses not listed in the exhibits to this order may 
be called only if the necessity of their testimony could not reasonably 
be foreseen ten (10) days prior to trial. If it appears to counsel at 
any time before trial that such rebuttal witnesses will be called, 
notice will immediately be given to opposing counsel and the Presiding 
Officer.
    7.3 The probable length of hearing is ---- days. The hearing will 
commence on the ---- day of --------, 19--, at -- o'clock -- m. at ----
----.
    7.4 Prehearing briefs will be filed not later than 5:00 p.m. on ----
---- (Insert date not later than ten (10) days prior to the hearing.) 
All anticipated legal questions, including those relating to the 
admissibility of evidence, must be covered by prehearing briefs.
    This prehearing order has been formulated after a conference at 
which counsel for the respective parties appeared. Reasonable 
opportunity has been afforded counsel for corrections or additions prior 
to signing. It will control the course of the hearing, and it may not be 
amended except by consent of the parties and the Presiding Officer, or 
by order of the Presiding Officer to prevent manifest injustice.
________________________________________________________________________
Presiding Officer.
Dated:__________________________________________________________________
Approved as to Form and Substance
Date:___________________________________________________________________
________________________________________________________________________
Complaint Counsel.
________________________________________________________________________
Attorney for Respondent(s)
________________________________________________________________________
*Attorney for Intervenors

    *Note: Where intervenors appear pursuant to Sec. 1025.17 of these 
Rules, the prehearing order may be suitably modified; the initial page 
may be modified to reflect the intervention.



PART 1027--SALARY OFFSET--Table of Contents




Sec.
1027.1 Purpose and scope.
1027.2 Definitions.
1027.3 Applicability.
1027.4 Notice requirements before offset.
1027.5 Hearing.
1027.6 Written decision.
1027.7 Coordinating offset with another Federal agency.
1027.8 Procedures for salary offset.
1027.9 Refunds.
1027.10 Statute of limitations.
1027.11 Non-waiver of rights.
1027.12 Interest, penalties, and administrative costs.

    Authority: 5 U.S.C. 5514, E.O. 11809 (redesignated E.O. 12107), and 
5 CFR part 550, subpart K.

    Source: 55 FR 34904, Aug. 27, 1990, unless otherwise noted.



Sec. 1027.1  Purpose and scope.

    (a) This regulation provides procedures for the collection by 
administrative offset of a Federal employee's salary without his/her 
consent to satisfy certain debts owed to the Federal government. These 
regulations apply to all Federal employees who owe debts to the Consumer 
Product Safety Commission (CPSC) and to current employees of CPSC who 
owe debts to other Federal agencies. This regulation does not apply when 
the employee consents to recovery from his/her current pay account.
    (b) This regulation does not apply to debts or claims arising under:
    (1) The Internal Revenue Code of 1954, as amended, 26 U.S.C. 1 et 
seq.;
    (2) The Social Security Act, 42 U.S.C. 301 et seq.;
    (3) The tariff laws of the United States; or
    (4) Any case where a collection of a debt by salary offset is 
explicitly provided for or prohibited by another statute.
    (c) This regulation does not apply to any adjustment to pay arising 
out of an employee's selecton of coverage or a change in coverage under 
a Federal benefits program requiring periodic deductions from pay if the 
amount to be recovered was accumulated over four pay periods or less.
    (d) This regulation does not preclude the compromise, suspension, or 
termination of collection action where appropriate under the standards 
implementing the Federal Claims Collection Act, 31 U.S.C. 3711 et seq., 
and 4 CFR parts 101 through 105.
    (e) This regulation does not preclude an employee from requesting 
waiver of an overpayment under 5 U.S.C. 5584, 10 U.S.C. 2774, or 32 
U.S.C. 716, or in any way questioning the amount or validity of the debt 
by submitting a subsequent claim to the General Accounting

[[Page 105]]

Office. This regulation does not preclude an employee from requesting a 
waiver pursuant to other statutory provisions applicable to the 
particular debt being collected.
    (f) Matters not addressed in these regulations should be reviewed in 
accordance with the Federal Claims Collection Standards at 4 CFR 101.1 
et seq.



Sec. 1027.2  Definitions.

    For the purposes of this part the following definitions will apply:
    Agency means an executive agency as defined at 5 U.S.C. 105, 
including the U.S. Postal Service and the U.S. Postal Rate Commission; a 
military department as defined at 5 U.S.C. 102; an agency or court in 
the judicial branch; an agency of the legislative branch, including the 
U.S. Senate and House of Representatives; and other independent 
establishments that are entities of the Federal government.
    Certification means a written debt claim received from a creditor 
agency which requests the paying agency to offset the salary of an 
employee.
    CPSC or Commission means the Consumer Product Safety Commission.
    Creditor agency means an agency of the Federal Government to which 
the debt is owed.
    Debt means an amount owed by a Federal employee to the United States 
from sources which include loans insured or guaranteed by the United 
States and all other amounts due the United States from fees, leases, 
rents, royalties, services, sales of real or personal property, 
overpayments, penalties, damages, interests, fines, forfeitures (except 
those arising under the Uniform Code of Military Justice), and all other 
similar sources.
    Disposable pay means the amount that remains from an employee's 
Federal pay after required deductions for social security, Federal, 
State or local income tax, health insurance premiums, retirement 
contributions, life insurance premiums, Federal employment taxes, and 
any other deductions that are required to be withheld by law.
    Executive Director means the Executive Director of the Consumer 
Product Safety Commission, who is the person designated by the Chairman 
to determine whether an employee is indebted to the United States and to 
take action to collect such debts.
    Hearing official means an individual responsible for conducting a 
hearing with respect to the existence or amount of a debt claimed, or 
the repayment schedule of a debt, and who renders a decision on the 
basis of such hearing. A hearing official may not be under the 
supervision or control of the Chairman of the Commission.
    Paying agency means the agency that employs the individual who owes 
the debt and authorizes the payments of his/her current pay.
    Salary offset means an administrative offset to collect a debt 
pursuant to 5 U.S.C. 5514 by deduction(s) at one or more officially 
established pay intervals from the current pay account of an employee 
without his/her consent.



Sec. 1027.3  Applicability.

    (a) These regulations are to be followed when:
    (1) The Commission is owed a debt by an individual who is a current 
employee of the CPSC; or
    (2) The Commission is owed a debt by an individual currently 
employed by another Federal agency; or
    (3) The Commission employs an individual who owes a debt to another 
federal agency.



Sec. 1027.4  Notice requirements before offset.

    (a) Salary offset shall not be made against an employee's pay unless 
the employee is provided with written notice signed by the Executive 
Director of the debt at least 30 days before salary offset commences.
    (b) The written notice shall contain:
    (1) A statement that the debt is owed and an explanation of its 
nature and amount;
    (2) The agency's intention to collect the debt by deducting from the 
employee's current disposable pay account;
    (3) The amount, frequency, proposed beginning date, and duration of 
the intended deduction(s);
    (4) An explanation of interest, penalties, and administrative 
charges, including a statement that such charges

[[Page 106]]

will be assessed unless excused in accordance with the Federal Claims 
Collections Standards at 4 CFR 101.1 et seq.;
    (5) The employee's right to inspect, request, and receive a copy of 
government records relating to the debt;
    (6) The employee's opportunity to establish a written schedule for 
the voluntary repayment of the debt in lieu of offset;
    (7) The employee's right to an oral hearing or a determination based 
on a review of the written record (``paper hearing'') conducted by an 
impartial hearing official concerning the existence or the amount of the 
debt, or the terms of the repayment schedule;
    (8) The procedures and time period for petitioning for a hearing;
    (9) A statement that a timely filing of a petition for a hearing 
will stay the commencement of collection proceedings;
    (10) A statement that a final decision on the hearing (if requested) 
will be issued by the hearing official not later than 60 days after the 
filing of the petition requesting the hearing unless the employee 
requests and the hearing official grants a delay in the proceedings;
    (11) A statement that knowingly false or frivolous statements, 
representations, or evidence may subject the employee to appropriate 
disciplinary procedures and/or statutory penalties;
    (12) A statement of other rights and remedies available to the 
employee under statutes or regulations governing the program for which 
the collection is being made;
    (13) Unless there are contractual or statutory provisions to the 
contrary, a statement that amounts paid on or deducted for the debt 
which are later waived or found not owed to the United States will be 
promptly refunded to the employee; and
    (14) A statement that the proceedings regarding such debt are 
governed by section 5 of the Debt Collection Act of 1982 (5 U.S.C. 
5514).



Sec. 1027.5  Hearing.

    (a) Request for hearing. (1) An employee may file a petition for an 
oral or paper hearing in accordance with the instructions outlined in 
the agency's notice to offset.
    (2) A hearing may be requested by filing a written petition 
addressed to the Executive Director stating why the employee disputes 
the existence or amount of the debt or, in the case of an individual 
whose repayment schedule has been established other than by a written 
agreement, concerning the terms of the repayment schedule. The petition 
for a hearing must be received by the Executive Director not later than 
fifteen (15) calendar days after the employee's receipt of the offset 
notice, or notice of the terms of the payment schedule, unless the 
employee can show good cause for failing to meet the filing deadline.
    (b) Hearing procedures. (1) The hearing will be presided over by an 
impartial hearing official.
    (2) The hearing shall conform to procedures contained in the Federal 
Claims Collection Standards, 4 CFR 102.3(c). The burden shall be on the 
employee to demonstrate that the existence or the amount of the debt is 
in error.



Sec. 1027.6  Written decision.

    (a) The hearing official shall issue a final written opinion no 
later than 60 days after the filing of the petition.
    (b) The written opinion will include: A statement of the facts 
presented to demonstrate the nature and origin of the alleged debt; the 
hearing official's analysis, findings, and conclusions; the amount and 
validity of the debt; and the repayment schedule.



Sec. 1027.7  Coordinating offset with another Federal agency.

    (a) The CPSC as the creditor agency. (1) When the Executive Director 
determines that an employee of another agency (i.e., the paying agency) 
owes a debt to the CPSC, the Executive Director shall, as appropriate:
    (i) Certify in writing to the paying agency that the employee owes 
the debt, the amount and basis of the debt, the date on which payment 
was due, and the date the Government's right to collect the debt 
accrued, and that this part 1027 has been approved by the Office of 
Personnel Management.
    (ii) Unless the employee has consented to salary offset in writing 
or

[[Page 107]]

signed a statement acknowledging receipt of the required procedures, and 
the written consent is sent to the paying agency, the Executive Director 
must advise the paying agency of the action(s) taken under this part 
1027, and the date(s) they were taken.
    (iii) Request the paying agency to collect the debt by salary 
offset. If deductions must be made in installments, the Executive 
Director may recommend to the paying agency the amount or percentage of 
disposable pay to be collected in each installment;
    (iv) Arrange for a hearing upon the proper petitioning by the 
employee;
    (v) If the employee is in the process of separating from the Federal 
service, the CPSC must submit its debt claim to the paying agency as 
provided in this part. The paying agency must certify the total amount 
collected, give a copy of the certification to the employee, and send a 
copy of the certification and notice of the employee's separation to the 
CPSC. If the paying agency is aware that the employee is entitled to 
Civil Service Retirement and Disability Fund or other similar payments, 
it must certify to the agency responsible for making such payments that 
the debtor owes a debt, including the amount of the debt, and that the 
provisions of 5 CFR 550.1108 have been followed; and
    (vi) If the employee has already separated from federal service and 
all payments due from the paying agency have been paid, the Executive 
Director may request, unless otherwise prohibited, that money payable to 
the employee from the Civil Service Retirement and Disability Fund or 
other similar funds be collected by administrative offset.
    (2) [Reserved]
    (b) The CPSC as the paying agency. (1) Upon receipt of a properly 
certified debt claim from another agency, deductions will be scheduled 
to begin at the next established pay interval. The employee must receive 
written notice that CPSC has received a certified debt claim from the 
creditor agency, the amount of the debt, the date salary offset will 
begin, and the amount of the deduction(s). CPSC shall not review the 
merits of the creditor agency's determination of the validity or the 
amount of the certified claim.
    (2) If the employee transfers to another agency after the creditor 
agency has submitted its debt claim to CPSC and before the debt is 
collected completely, CPSC must certify the amount collected. One copy 
of the certification must be furnished to the employee. A copy must be 
furnished to the creditor agency with notice of the employee's transfer.



Sec. 1027.8  Procedures for salary offset.

    (a) Deductions to liquidate an employee's debt will be by the method 
and in the amount stated in the Executive Director's notice of intention 
to offset as provided in Sec. 1027.4. Debts will be collected in one 
lump sum where possible. If the employee is financially unable to pay in 
one lump sum, collection must be made in installments.
    (b) Debts will be collected by deduction at officially established 
pay intervals from an employee's current pay account unless alternative 
arrangements for repayment are made.
    (c) Installment deductions will be made over a period not greater 
than the anticipated period of employment. The size of installment 
deductions must bear a reasonable relationship to the size of the debt 
and the employee's ability to pay. The deduction for the pay intervals 
for any period must not exceed 15% of disposable pay unless the employee 
has agreed in writing to a deduction of a greater amount.
    (d) Unliquidated debts may be offset against any financial payment 
due to a separated employee including but not limited to final salary or 
leave payment in accordance with 31 U.S.C. 3716.



Sec. 1027.9  Refunds.

    (a) CPSC will promptly refund to an employee any amounts deducted to 
satisfy debts owed to CPSC when the debt is waived, found not owed to 
CPSC, or when directed by an administrative or judicial order.
    (b) Another creditor agency will promptly return to CPSC any amounts 
deducted by CPSC to satisfy debts owed to the creditor agency when the 
debt is waived, found not owed, or when directed by an administrative or 
judicial order.

[[Page 108]]

    (c) Unless required by law, refunds under this paragraph shall not 
bear interest.



Sec. 1027.10  Statute of limitations.

    (a) If a debt has been outstanding for more than 10 years after 
CPSC's right to collect the debt first accrued, the agency may not 
collect by salary offset unless facts material to the Government's right 
to collect were not known and could not reasonably have been known by 
the official or officials who were charged with the responsibility for 
discovery and collection of such debts.
    (b) [Reserved]



Sec. 1027.11  Non-waiver of rights.

    An employee's involuntary payment of all or any part of a debt 
collected under these regulations will not be construed as a waiver of 
any rights that the employee may have under 5 U.S.C. 5514 or any other 
provision of law.



Sec. 1027.12  Interest, penalties, and administrative costs.

    Charges may be assessed on a debt for interest, penalties, and 
administrative costs in accordance with 31 U.S.C. 3717 and the Federal 
Claims Collection Standards, 4 CFR 101.1 et seq.



PART 1028--PROTECTION OF HUMAN SUBJECTS--Table of Contents




Sec.
1028.101 To what does this policy apply?
1028.102 Definitions.
1028.103 Assuring compliance with this policy--research conducted or 
          supported by any Federal Department or Agency.
1028.104-1028.106 [Reserved]
1028.107 IRB membership.
1028.108 IRB functions and operations.
1028.109 IRB review of research.
1028.110 Expedited review procedures for certain kinds of research 
          involving no more than minimal risk, and for minor changes in 
          approved research.
1028.111 Criteria for IRB approval of research.
1028.112 Review by institution.
1028.113 Suspension or termination of IRB approval of research.
1028.114 Cooperative research.
1028.115 IRB records.
1028.116 General requirements for informed consent.
1028.117 Documentation of informed consent.
1028.118 Applications and proposals lacking definite plans for 
          involvement of human subjects.
1028.119 Research undertaken without the intention of involving human 
          subjects.
1028.120 Evaluation and disposition of applications and proposals for 
          research to be conducted or supported by a Federal Department 
          or Agency.
1028.121 [Reserved]
1028.122 Use of Federal funds.
1028.123 Early termination of research support: Evaluation of 
          applications and proposals.
1028.124 Conditions.

    Authority: 5 U.S.C. 301; 42 U.S.C. 300v-1(b).

    Source: 56 FR 28012, 28019, June 18, 1991, unless otherwise noted.



Sec. 1028.101  To what does this policy apply?

    (a) Except as provided in paragraph (b) of this section, this policy 
applies to all research involving human subjects conducted, supported or 
otherwise subject to regulation by any federal department or agency 
which takes appropriate administrative action to make the policy 
applicable to such research. This includes research conducted by federal 
civilian employees or military personnel, except that each department or 
agency head may adopt such procedural modifications as may be 
appropriate from an administrative standpoint. It also includes research 
conducted, supported, or otherwise subject to regulation by the federal 
government outside the United States.
    (1) Research that is conducted or supported by a federal department 
or agency, whether or not it is regulated as defined in 
Sec. 1028.102(e), must comply with all sections of this policy.
    (2) Research that is neither conducted nor supported by a federal 
department or agency but is subject to regulation as defined in 
Sec. 1028.102(e) must be reviewed and approved, in compliance with 
Sec. Sec. 1028.101, 1028.102, and 1028.107 through 1028.117 of this 
policy, by an institutional review board (IRB) that operates in 
accordance with the pertinent requirements of this policy.
    (b) Unless otherwise required by department or agency heads, 
research activities in which the only involvement of human subjects will 
be in one or

[[Page 109]]

more of the following categories are exempt from this policy:
    (1) Research conducted in established or commonly accepted 
educational settings, involving normal educational practices, such as 
(i) research on regular and special education instructional strategies, 
or (ii) research on the effectiveness of or the comparison among 
instructional techniques, curricula, or classroom management methods.
    (2) Research involving the use of educational tests (cognitive, 
diagnostic, aptitude, achievement), survey procedures, interview 
procedures or observation of public behavior, unless:
    (i) Information obtained is recorded in such a manner that human 
subjects can be identified, directly or through identifiers linked to 
the subjects; and
    (ii) Any disclosure of the human subjects' responses outside the 
research could reasonably place the subjects at risk of criminal or 
civil liability or be damaging to the subjects' financial standing, 
employability, or reputation.
    (3) Research involving the use of educational tests (cognitive, 
diagnostic, aptitude, achievement), survey procedures, interview 
procedures, or observation of public behavior that is not exempt under 
paragraph (b)(2) of this section, if:
    (i) The human subjects are elected or appointed public officials or 
candidates for public office; or
    (ii) Federal statute(s) require(s) without exception that the 
confidentiality of the personally identifiable information will be 
maintained throughout the research and thereafter.
    (4) Research, involving the collection or study of existing data, 
documents, records, pathological specimens, or diagnostic specimens, if 
these sources are publicly available or if the information is recorded 
by the investigator in such a manner that subjects cannot be identified, 
directly or through identifiers linked to the subjects.
    (5) Research and demonstration projects which are conducted by or 
subject to the approval of department or agency heads, and which are 
designed to study, evaluate, or otherwise examine:
    (i) Public benefit or service programs;
    (ii) Procedures for obtaining benefits or services under those 
programs;
    (iii) Possible changes in or alternatives to those programs or 
procedures; or
    (iv) Possible changes in methods or levels of payment for benefits 
or services under those programs.
    (6) Taste and food quality evaluation and consumer acceptance 
studies, (i) if wholesome foods without additives are consumed or (ii) 
if a food is consumed that contains a food ingredient at or below the 
level and for a use found to be safe, or agricultural chemical or 
environmental contaminant at or below the level found to be safe, by the 
Food and Drug Administration or approved by the Environmental Protection 
Agency or the Food Safety and Inspection Service of the U.S. Department 
of Agriculture.
    (c) Department or agency heads retain final judgment as to whether a 
particular activity is covered by this policy.
    (d) Department or agency heads may require that specific research 
activities or classes of research activities conducted, supported, or 
otherwise subject to regulation by the department or agency but not 
otherwise covered by this policy, comply with some or all of the 
requirements of this policy.
    (e) Compliance with this policy requires compliance with pertinent 
federal laws or regulations which provide additional protections for 
human subjects.
    (f) This policy does not affect any state or local laws or 
regulations which may otherwise be applicable and which provide 
additional protections for human subjects.
    (g) This policy does not affect any foreign laws or regulations 
which may otherwise be applicable and which provide additional 
protections to human subjects of research.
    (h) When research covered by this policy takes place in foreign 
countries, procedures normally followed in the foreign countries to 
protect human subjects may differ from those set forth in this policy. 
(An example is a foreign institution which complies with guidelines 
consistent with the World Medical Assembly Declaration (Declaration of 
Helsinki amended 1989)

[[Page 110]]

issued either by sovereign states or by an organization whose function 
for the protection of human research subjects is internationally 
recognized.) In these circumstances, if a department or agency head 
determines that the procedures prescribed by the institution afford 
protections that are at least equivalent to those provided in this 
policy, the department or agency head may approve the substitution of 
the foreign procedures in lieu of the procedural requirements provided 
in this policy. Except when otherwise required by statute, Executive 
Order, or the department or agency head, notices of these actions as 
they occur will be published in the Federal Register or will be 
otherwise published as provided in department or agency procedures.
    (i) Unless otherwise required by law, department or agency heads may 
waive the applicability of some or all of the provisions of this policy 
to specific research activities or classes of research activities 
otherwise covered by this policy. Except when otherwise required by 
statute or Executive Order, the department or agency head shall forward 
advance notices of these actions to the Office for Protection from 
Research Risks, Department of Health and Human Services (HHS), and shall 
also publish them in the Federal Register or in such other manner as 
provided in department or agency procedures. \1\
---------------------------------------------------------------------------

    \1\ Institutions with HHS-approved assurances on file will abide by 
provisions of title 45 CFR part 46, subparts A-D. Some of the other 
Departments and Agencies have incorporated all provisions of title 45 
CFR part 46 into their policies and procedures as well. However, the 
exemptions at 45 CFR 46.101(b) do not apply to research involving 
prisoners, fetuses, pregnant women, or human in vitro fertilization, 
subparts B and C. The exemption at 45 CFR 46.101(b)(2), for research 
involving survey or interview procedures or observation of public 
behavior, does not apply to research with children, subpart D, except 
for research involving observations of public behavior when the 
investigator(s) do not participate in the activities being observed.

[56 FR 28012, 28019, June 18, 1991; 56 FR 29756, June 28, 1991]



Sec. 1028.102  Definitions.

    (a) Department or agency head means the head of any federal 
department or agency and any other officer or employee of any department 
or agency to whom authority has been delegated.
    (b) Institution means any public or private entity or agency 
(including federal, state, and other agencies).
    (c) Legally authorized representative means an individual or 
judicial or other body authorized under applicable law to consent on 
behalf of a prospective subject to the subject's participation in the 
procedure(s) involved in the research.
    (d) Research means a systematic investigation, including research 
development, testing and evaluation, designed to develop or contribute 
to generalizable knowledge. Activities which meet this definition 
constitute research for purposes of this policy, whether or not they are 
conducted or supported under a program which is considered research for 
other purposes. For example, some demonstration and service programs may 
include research activities.
    (e) Research subject to regulation, and similar terms are intended 
to encompass those research activities for which a federal department or 
agency has specific responsibility for regulating as a research 
activity, (for example, Investigational New Drug requirements 
administered by the Food and Drug Administration). It does not include 
research activities which are incidentally regulated by a federal 
department or agency solely as part of the department's or agency's 
broader responsibility to regulate certain types of activities whether 
research or non-research in nature (for example, Wage and Hour 
requirements administered by the Department of Labor).
    (f) Human subject means a living individual about whom an 
investigator (whether professional or student) conducting research 
obtains:
    (1) Data through intervention or interaction with the individual, or
    (2) Identifiable private information.

Intervention includes both physical procedures by which data are 
gathered (for example, venipuncture) and manipulations of the subject or 
the subject's environment that are performed for research purposes. 
Interaction includes communication or interpersonal contact between 
investigator and subject.

[[Page 111]]

``Private information'' includes information about behavior that occurs 
in a context in which an individual can reasonably expect that no 
observation or recording is taking place, and information which has been 
provided for specific purposes by an individual and which the individual 
can reasonably expect will not be made public (for example, a medical 
record). Private information must be individually identifiable (i.e., 
the identity of the subject is or may readily be ascertained by the 
investigator or associated with the information) in order for obtaining 
the information to constitute research involving human subjects.
    (g) IRB means an institutional review board established in accord 
with and for the purposes expressed in this policy.
    (h) IRB approval means the determination of the IRB that the 
research has been reviewed and may be conducted at an institution within 
the constraints set forth by the IRB and by other institutional and 
federal requirements.
    (i) Minimal risk means that the probability and magnitude of harm or 
discomfort anticipated in the research are not greater in and of 
themselves than those ordinarily encountered in daily life or during the 
performance of routine physical or psychological examinations or tests.
    (j) Certification means the official notification by the institution 
to the supporting department or agency, in accordance with the 
requirements of this policy, that a research project or activity 
involving human subjects has been reviewed and approved by an IRB in 
accordance with an approved assurance.



Sec. 1028.103  Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency.

    (a) Each institution engaged in research which is covered by this 
policy and which is conducted or supported by a Federal department or 
agency shall provide written assurance satisfactory to the department or 
agency head that it will comply with the requirements set forth in this 
policy. In lieu of requiring submission of an assurance, individual 
department or agency heads shall accept the existence of a current 
assurance, appropriate for the research in question, on file with the 
Office for Protection from Research Risks, HHS, and approved for 
federalwide use by that office. When the existence of an HHS-approved 
assurance is accepted in lieu of requiring submission of an assurance, 
reports (except certification) required by this policy to be made to 
department and agency heads shall also be made to the Office for 
Protection from Research Risks, HHS.
    (b) Departments and agencies will conduct or support research 
covered by this policy only if the institution has an assurance approved 
as provided in this section, and only if the institution has certified 
to the department or agency head that the research has been reviewed and 
approved by an IRB provided for in the assurance, and will be subject to 
continuing review by the IRB. Assurances applicable to federally 
supported or conducted research shall at a minimum include:
    (1) A statement of principles governing the institution in the 
discharge of its responsibilities for protecting the rights and welfare 
of human subjects of research conducted at or sponsored by the 
institution, regardless of whether the research is subject to federal 
regulation. This may include an appropriate existing code, declaration, 
or statement of ethical principles, or a statement formulated by the 
institution itself. This requirement does not preempt provisions of this 
policy applicable to department- or agency-supported or regulated 
research and need not be applicable to any research exempted or waived 
under Sec. 1028.101 (b) or (i).
    (2) Designation of one or more IRBs established in accordance with 
the requirements of this policy, and for which provisions are made for 
meeting space and sufficient staff to support the IRB's review and 
recordkeeping duties.
    (3) A list of IRB members identified by name; earned degrees; 
representative capacity; indications of experience such as board 
certifications, licenses, etc., sufficient to describe each member's 
chief anticipated contributions to IRB deliberations; and any employment 
or other relationship between

[[Page 112]]

each member and the institution; for example: full-time employee, part-
time employee, member of governing panel or board, stockholder, paid or 
unpaid consultant. Changes in IRB membership shall be reported to the 
department or agency head, unless in accord with Sec. 1028.103(a) of 
this policy, the existence of an HHS-approved assurance is accepted. In 
this case, change in IRB membership shall be reported to the Office for 
Protection from Research Risks, HHS.
    (4) Written procedures which the IRB will follow:
    (i) For conducting its initial and continuing review of research and 
for reporting its findings and actions to the investigator and the 
institution;
    (ii) For determining which projects require review more often than 
annually and which projects need verification from sources other than 
the investigators that no material changes have occurred since previous 
IRB review; and
    (iii) For ensuring prompt reporting to the IRB of proposed changes 
in a research activity, and for ensuring that such changes in approved 
research, during the period for which IRB approval has already been 
given, may not be initiated without IRB review and approval except when 
necessary to eliminate apparent immediate hazards to the subject.
    (5) Written procedures for ensuring prompt reporting to the IRB, 
appropriate institutional officials, and the department or agency head 
of (i) any unanticipated problems involving risks to subjects or others 
or any serious or continuing noncompliance with this policy or the 
requirements or determinations of the IRB and (ii) any suspension or 
termination of IRB approval.
    (c) The assurance shall be executed by an individual authorized to 
act for the institution and to assume on behalf of the institution the 
obligations imposed by this policy and shall be filed in such form and 
manner as the department or agency head prescribes.
    (d) The department or agency head will evaluate all assurances 
submitted in accordance with this policy through such officers and 
employees of the department or agency and such experts or consultants 
engaged for this purpose as the department or agency head determines to 
be appropriate. The department or agency head's evaluation will take 
into consideration the adequacy of the proposed IRB in light of the 
anticipated scope of the institution's research activities and the types 
of subject populations likely to be involved, the appropriateness of the 
proposed initial and continuing review procedures in light of the 
probable risks, and the size and complexity of the institution.
    (e) On the basis of this evaluation, the department or agency head 
may approve or disapprove the assurance, or enter into negotiations to 
develop an approvable one. The department or agency head may limit the 
period during which any particular approved assurance or class of 
approved assurances shall remain effective or otherwise condition or 
restrict approval.
    (f) Certification is required when the research is supported by a 
federal department or agency and not otherwise exempted or waived under 
Sec. 1028.101 (b) or (i). An institution with an approved assurance 
shall certify that each application or proposal for research covered by 
the assurance and by Sec. 1028.103 of this Policy has been reviewed and 
approved by the IRB. Such certification must be submitted with the 
application or proposal or by such later date as may be prescribed by 
the department or agency to which the application or proposal is 
submitted. Under no condition shall research covered by Sec. 1028.103 of 
the Policy be supported prior to receipt of the certification that the 
research has been reviewed and approved by the IRB. Institutions without 
an approved assurance covering the research shall certify within 30 days 
after receipt of a request for such a certification from the department 
or agency, that the application or proposal has been approved by the 
IRB. If the certification is not submitted within these time limits, the 
application or proposal may be returned to the institution.

(Approved by the Office of Management and Budget under control number 
9999-0020)

[56 FR 28012, 28019, June 18, 1991; 56 FR 29756, June 28, 1991]

[[Page 113]]



Sec. Sec. 1028.104-1028.106  [Reserved]



Sec. 1028.107  IRB membership.

    (a) Each IRB shall have at least five members, with varying 
backgrounds to promote complete and adequate review of research 
activities commonly conducted by the institution. The IRB shall be 
sufficiently qualified through the experience and expertise of its 
members, and the diversity of the members, including consideration of 
race, gender, and cultural backgrounds and sensitivity to such issues as 
community attitudes, to promote respect for its advice and counsel in 
safeguarding the rights and welfare of human subjects. In addition to 
possessing the professional competence necessary to review specific 
research activities, the IRB shall be able to ascertain the 
acceptability of proposed research in terms of institutional commitments 
and regulations, applicable law, and standards of professional conduct 
and practice. The IRB shall therefore include persons knowledgeable in 
these areas. If an IRB regularly reviews research that involves a 
vulnerable category of subjects, such as children, prisoners, pregnant 
women, or handicapped or mentally disabled persons, consideration shall 
be given to the inclusion of one or more individuals who are 
knowledgeable about and experienced in working with these subjects.
    (b) Every nondiscriminatory effort will be made to ensure that no 
IRB consists entirely of men or entirely of women, including the 
institution's consideration of qualified persons of both sexes, so long 
as no selection is made to the IRB on the basis of gender. No IRB may 
consist entirely of members of one profession.
    (c) Each IRB shall include at least one member whose primary 
concerns are in scientific areas and at least one member whose primary 
concerns are in nonscientific areas.
    (d) Each IRB shall include at least one member who is not otherwise 
affiliated with the institution and who is not part of the immediate 
family of a person who is affiliated with the institution.
    (e) No IRB may have a member participate in the IRB's initial or 
continuing review of any project in which the member has a conflicting 
interest, except to provide information requested by the IRB.
    (f) An IRB may, in its discretion, invite individuals with 
competence in special areas to assist in the review of issues which 
require expertise beyond or in addition to that available on the IRB. 
These individuals may not vote with the IRB.



Sec. 1028.108  IRB functions and operations.

    In order to fulfill the requirements of this policy each IRB shall:
    (a) Follow written procedures in the same detail as described in 
Sec. 1028.103(b)(4) and, to the extent required by, Sec. 1028.103(b)(5).
    (b) Except when an expedited review procedure is used (see 
Sec. 1028.110), review proposed research at convened meetings at which a 
majority of the members of the IRB are present, including at least one 
member whose primary concerns are in nonscientific areas. In order for 
the research to be approved, it shall receive the approval of a majority 
of those members present at the meeting.



Sec. 1028.109  IRB review of research.

    (a) An IRB shall review and have authority to approve, require 
modifications in (to secure approval), or disapprove all research 
activities covered by this policy.
    (b) An IRB shall require that information given to subjects as part 
of informed consent is in accordance with Sec. 1028.116. The IRB may 
require that information, in addition to that specifically mentioned in 
Sec. 1028.116, be given to the subjects when in the IRB's judgment the 
information would meaningfully add to the protection of the rights and 
welfare of subjects.
    (c) An IRB shall require documentation of informed consent or may 
waive documentation in accordance with Sec. 1028.117.
    (d) An IRB shall notify investigators and the institution in writing 
of its decision to approve or disapprove the proposed research activity, 
or of modifications required to secure IRB approval of the research 
activity. If the IRB decides to disapprove a research activity,

[[Page 114]]

it shall include in its written notification a statement of the reasons 
for its decision and give the investigator an opportunity to respond in 
person or in writing.
    (e) An IRB shall conduct continuing review of research covered by 
this policy at intervals appropriate to the degree of risk, but not less 
than once per year, and shall have authority to observe or have a third 
party observe the consent process and the research.

(Approved by the Office of Management and Budget under control number 
9999-0020)



Sec. 1028.110  Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.

    (a) The Secretary, HHS, has established, and published as a Notice 
in the Federal Register, a list of categories of research that may be 
reviewed by the IRB through an expedited review procedure. The list will 
be amended, as appropriate after consultation with other departments and 
agencies, through periodic republication by the Secretary, HHS, in the 
Federal Register. A copy of the list is available from the Office for 
Protection from Research Risks, National Institutes of Health, HHS, 
Bethesda, Maryland 20892.
    (b) An IRB may use the expedited review procedure to review either 
or both of the following:
    (1) Some or all of the research appearing on the list and found by 
the reviewer(s) to involve no more than minimal risk,
    (2) Minor changes in previously approved research during the period 
(of one year or less) for which approval is authorized.

Under an expedited review procedure, the review may be carried out by 
the IRB chairperson or by one or more experienced reviewers designated 
by the chairperson from among members of the IRB. In reviewing the 
research, the reviewers may exercise all of the authorities of the IRB 
except that the reviewers may not disapprove the research. A research 
activity may be disapproved only after review in accordance with the 
non-expedited procedure set forth in Sec. 1028.108(b).
    (c) Each IRB which uses an expedited review procedure shall adopt a 
method for keeping all members advised of research proposals which have 
been approved under the procedure.
    (d) The department or agency head may restrict, suspend, terminate, 
or choose not to authorize an institution's or IRB's use of the 
expedited review procedure.



Sec. 1028.111  Criteria for IRB approval of research.

    (a) In order to approve research covered by this policy the IRB 
shall determine that all of the following requirements are satisfied:
    (1) Risks to subjects are minimized:
    (i) By using procedures which are consistent with sound research 
design and which do not unnecessarily expose subjects to risk, and
    (ii) Whenever appropriate, by using procedures already being 
performed on the subjects for diagnostic or treatment purposes.
    (2) Risks to subjects are reasonable in relation to anticipated 
benefits, if any, to subjects, and the importance of the knowledge that 
may reasonably be expected to result. In evaluating risks and benefits, 
the IRB should consider only those risks and benefits that may result 
from the research (as distinguished from risks and benefits of therapies 
subjects would receive even if not participating in the research). The 
IRB should not consider possible long-range effects of applying 
knowledge gained in the research (for example, the possible effects of 
the research on public policy) as among those research risks that fall 
within the purview of its responsibility.
    (3) Selection of subjects is equitable. In making this assessment 
the IRB should take into account the purposes of the research and the 
setting in which the research will be conducted and should be 
particularly cognizant of the special problems of research involving 
vulnerable populations, such as children, prisoners, pregnant women, 
mentally disabled persons, or economically or educationally 
disadvantaged persons.
    (4) Informed consent will be sought from each prospective subject or 
the

[[Page 115]]

subject's legally authorized representative, in accordance with, and to 
the extent required by Sec. 1028.116.
    (5) Informed consent will be appropriately documented, in accordance 
with, and to the extent required by Sec. 1028.117.
    (6) When appropriate, the research plan makes adequate provision for 
monitoring the data collected to ensure the safety of subjects.
    (7) When appropriate, there are adequate provisions to protect the 
privacy of subjects and to maintain the confidentiality of data.
    (b) When some or all of the subjects are likely to be vulnerable to 
coercion or undue influence, such as children, prisoners, pregnant 
women, mentally disabled persons, or economically or educationally 
disadvantaged persons, additional safeguards have been included in the 
study to protect the rights and welfare of these subjects.



Sec. 1028.112  Review by institution.

    Research covered by this policy that has been approved by an IRB may 
be subject to further appropriate review and approval or disapproval by 
officials of the institution. However, those officials may not approve 
the research if it has not been approved by an IRB.



Sec. 1028.113  Suspension or termination of IRB approval of research.

    An IRB shall have authority to suspend or terminate approval of 
research that is not being conducted in accordance with the IRB's 
requirements or that has been associated with unexpected serious harm to 
subjects. Any suspension or termination of approval shall include a 
statement of the reasons for the IRB's action and shall be reported 
promptly to the investigator, appropriate institutional officials, and 
the department or agency head.

(Approved by the Office of Management and Budget under control number 
9999-0020)



Sec. 1028.114  Cooperative research.

    Cooperative research projects are those projects covered by this 
policy which involve more than one institution. In the conduct of 
cooperative research projects, each institution is responsible for 
safeguarding the rights and welfare of human subjects and for complying 
with this policy. With the approval of the department or agency head, an 
institution participating in a cooperative project may enter into a 
joint review arrangement, rely upon the review of another qualified IRB, 
or make similar arrangements for avoiding duplication of effort.



Sec. 1028.115  IRB records.

    (a) An institution, or when appropriate an IRB, shall prepare and 
maintain adequate documentation of IRB activities, including the 
following:
    (1) Copies of all research proposals reviewed, scientific 
evaluations, if any, that accompany the proposals, approved sample 
consent documents, progress reports submitted by investigators, and 
reports of injuries to subjects.
    (2) Minutes of IRB meetings which shall be in sufficient detail to 
show attendance at the meetings; actions taken by the IRB; the vote on 
these actions including the number of members voting for, against, and 
abstaining; the basis for requiring changes in or disapproving research; 
and a written summary of the discussion of controverted issues and their 
resolution.
    (3) Records of continuing review activities.
    (4) Copies of all correspondence between the IRB and the 
investigators.
    (5) A list of IRB members in the same detail as described is 
Sec. 1028.103(b)(3).
    (6) Written procedures for the IRB in the same detail as described 
in Sec. Sec. 1028.103(b)(4) and 1028.103(b)(5).
    (7) Statements of significant new findings provided to subjects, as 
required by Sec. 1028.116(b)(5).
    (b) The records required by this policy shall be retained for at 
least 3 years, and records relating to research which is conducted shall 
be retained for at least 3 years after completion of the research. All 
records shall be accessible for inspection and copying by authorized 
representatives of the department or agency at reasonable times and in a 
reasonable manner.

(Approved by the Office of Management and Budget under control number 
9999-0020)

[[Page 116]]



Sec. 1028.116  General requirements for informed consent.

    Except as provided elsewhere in this policy, no investigator may 
involve a human being as a subject in research covered by this policy 
unless the investigator has obtained the legally effective informed 
consent of the subject or the subject's legally authorized 
representative. An investigator shall seek such consent only under 
circumstances that provide the prospective subject or the representative 
sufficient opportunity to consider whether or not to participate and 
that minimize the possibility of coercion or undue influence. The 
information that is given to the subject or the representative shall be 
in language understandable to the subject or the representative. No 
informed consent, whether oral or written, may include any exculpatory 
language through which the subject or the representative is made to 
waive or appear to waive any of the subject's legal rights, or releases 
or appears to release the investigator, the sponsor, the institution or 
its agents from liability for negligence.
    (a) Basic elements of informed consent. Except as provided in 
paragraph (c) or (d) of this section, in seeking informed consent the 
following information shall be provided to each subject:
    (1) A statement that the study involves research, an explanation of 
the purposes of the research and the expected duration of the subject's 
participation, a description of the procedures to be followed, and 
identification of any procedures which are experimental;
    (2) A description of any reasonably foreseeable risks or discomforts 
to the subject;
    (3) A description of any benefits to the subject or to others which 
may reasonably be expected from the research;
    (4) A disclosure of appropriate alternative procedures or courses of 
treatment, if any, that might be advantageous to the subject;
    (5) A statement describing the extent, if any, to which 
confidentiality of records identifying the subject will be maintained;
    (6) For research involving more than minimal risk, an explanation as 
to whether any compensation and an explanation as to whether any medical 
treatments are available if injury occurs and, if so, what they consist 
of, or where further information may be obtained;
    (7) An explanation of whom to contact for answers to pertinent 
questions about the research and research subjects' rights, and whom to 
contact in the event of a research-related injury to the subject; and
    (8) A statement that participation is voluntary, refusal to 
participate will involve no penalty or loss of benefits to which the 
subject is otherwise entitled, and the subject may discontinue 
participation at any time without penalty or loss of benefits to which 
the subject is otherwise entitled.
    (b) Additional elements of informed consent. When appropriate, one 
or more of the following elements of information shall also be provided 
to each subject:
    (1) A statement that the particular treatment or procedure may 
involve risks to the subject (or to the embryo or fetus, if the subject 
is or may become pregnant) which are currently unforeseeable;
    (2) Anticipated circumstances under which the subject's 
participation may be terminated by the investigator without regard to 
the subject's consent;
    (3) Any additional costs to the subject that may result from 
participation in the research;
    (4) The consequences of a subject's decision to withdraw from the 
research and procedures for orderly termination of participation by the 
subject;
    (5) A statement that significant new findings developed during the 
course of the research which may relate to the subject's willingness to 
continue participation will be provided to the subject; and
    (6) The approximate number of subjects involved in the study.
    (c) An IRB may approve a consent procedure which does not include, 
or which alters, some or all of the elements of informed consent set 
forth above, or waive the requirement to obtain informed consent 
provided the IRB finds and documents that:
    (1) The research or demonstration project is to be conducted by or 
subject

[[Page 117]]

to the approval of state or local government officials and is designed 
to study, evaluate, or otherwise examine:
    (i) Public benefit of service programs;
    (ii) Procedures for obtaining benefits or services under those 
programs;
    (iii) Possible changes in or alternatives to those programs or 
procedures; or
    (iv) Possible changes in methods or levels of payment for benefits 
or services under those programs; and
    (2) The research could not practicably be carried out without the 
waiver or alteration.
    (d) An IRB may approve a consent procedure which does not include, 
or which alters, some or all of the elements of informed consent set 
forth in this section, or waive the requirements to obtain informed 
consent provided the IRB finds and documents that:
    (1) The research involves no more than minimal risk to the subjects;
    (2) The waiver or alteration will not adversely affect the rights 
and welfare of the subjects;
    (3) The research could not practicably be carried out without the 
waiver or alteration; and
    (4) Whenever appropriate, the subjects will be provided with 
additional pertinent information after participation.
    (e) The informed consent requirements in this policy are not 
intended to preempt any applicable federal, state, or local laws which 
require additional information to be disclosed in order for informed 
consent to be legally effective.
    (f) Nothing in this policy is intended to limit the authority of a 
physician to provide emergency medical care, to the extent the physician 
is permitted to do so under applicable federal, state, or local law.

(Approved by the Office of Management and Budget under control number 
9999-0020)



Sec. 1028.117  Documentation of informed consent.

    (a) Except as provided in paragraph (c) of this section, informed 
consent shall be documented by the use of a written consent form 
approved by the IRB and signed by the subject or the subject's legally 
authorized representative. A copy shall be given to the person signing 
the form.
    (b) Except as provided in paragraph (c) of this section, the consent 
form may be either of the following:
    (1) A written consent document that embodies the elements of 
informed consent required by Sec. 1028.116. This form may be read to the 
subject or the subject's legally authorized representative, but in any 
event, the investigator shall give either the subject or the 
representative adequate opportunity to read it before it is signed; or
    (2) A short form written consent document stating that the elements 
of informed consent required by Sec. 1028.116 have been presented orally 
to the subject or the subject's legally authorized representative. When 
this method is used, there shall be a witness to the oral presentation. 
Also, the IRB shall approve a written summary of what is to be said to 
the subject or the representative. Only the short form itself is to be 
signed by the subject or the representative. However, the witness shall 
sign both the short form and a copy of the summary, and the person 
actually obtaining consent shall sign a copy of the summary. A copy of 
the summary shall be given to the subject or the representative, in 
addition to a copy of the short form.
    (c) An IRB may waive the requirement for the investigator to obtain 
a signed consent form for some or all subjects if it finds either:
    (1) That the only record linking the subject and the research would 
be the consent document and the principal risk would be potential harm 
resulting from a breach of confidentiality. Each subject will be asked 
whether the subject wants documentation linking the subject with the 
research, and the subject's wishes will govern; or
    (2) That the research presents no more than minimal risk of harm to 
subjects and involves no procedures for which written consent is 
normally required outside of the research context.
    In cases in which the documentation requirement is waived, the IRB 
may require the investigator to provide subjects with a written 
statement regarding the research.

(Approved by the Office of Management and Budget under control number 
9999-0020)

[[Page 118]]



Sec. 1028.118  Applications and proposals lacking definite plans for involvement of human subjects.

    Certain types of applications for grants, cooperative agreements, or 
contracts are submitted to departments or agencies with the knowledge 
that subjects may be involved within the period of support, but definite 
plans would not normally be set forth in the application or proposal. 
These include activities such as institutional type grants when 
selection of specific projects is the institution's responsibility; 
research training grants in which the activities involving subjects 
remain to be selected; and projects in which human subjects' involvement 
will depend upon completion of instruments, prior animal studies, or 
purification of compounds. These applications need not be reviewed by an 
IRB before an award may be made. However, except for research exempted 
or waived under Sec. 1028.101 (b) or (i), no human subjects may be 
involved in any project supported by these awards until the project has 
been reviewed and approved by the IRB, as provided in this policy, and 
certification submitted, by the institution, to the department or 
agency.



Sec. 1028.119  Research undertaken without the intention of involving human subjects.

    In the event research is undertaken without the intention of 
involving human subjects, but it is later proposed to involve human 
subjects in the research, the research shall first be reviewed and 
approved by an IRB, as provided in this policy, a certification 
submitted, by the institution, to the department or agency, and final 
approval given to the proposed change by the department or agency.



Sec. 1028.120  Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.

    (a) The department or agency head will evaluate all applications and 
proposals involving human subjects submitted to the department or agency 
through such officers and employees of the department or agency and such 
experts and consultants as the department or agency head determines to 
be appropriate. This evaluation will take into consideration the risks 
to the subjects, the adequacy of protection against these risks, the 
potential benefits of the research to the subjects and others, and the 
importance of the knowledge gained or to be gained.
    (b) On the basis of this evaluation, the department or agency head 
may approve or disapprove the application or proposal, or enter into 
negotiations to develop an approvable one.



Sec. 1028.121  [Reserved]



Sec. 1028.122  Use of Federal funds.

    Federal funds administered by a department or agency may not be 
expended for research involving human subjects unless the requirements 
of this policy have been satisfied.



Sec. 1028.123  Early termination of research support: Evaluation of applications and proposals.

    (a) The department or agency head may require that department or 
agency support for any project be terminated or suspended in the manner 
prescribed in applicable program requirements, when the department or 
agency head finds an institution has materially failed to comply with 
the terms of this policy.
    (b) In making decisions about supporting or approving applications 
or proposals covered by this policy the department or agency head may 
take into account, in addition to all other eligibility requirements and 
program criteria, factors such as whether the applicant has been subject 
to a termination or suspension under paragarph (a) of this section and 
whether the applicant or the person or persons who would direct or has 
have directed the scientific and technical aspects of an activity has 
have, in the judgment of the department or agency head, materially 
failed to discharge responsibility for the protection of the rights and 
welfare of human subjects (whether or not the research was subject to 
federal regulation).

[[Page 119]]



Sec. 1028.124  Conditions.

    With respect to any research project or any class of research 
projects the department or agency head may impose additional conditions 
prior to or at the time of approval when in the judgment of the 
department or agency head additional conditions are necessary for the 
protection of human subjects.



PART 1030--EMPLOYEE STANDARDS OF CONDUCT--Table of Contents




                           Subpart A--General

Sec.
1030.101 Cross-references to employee ethical conduct standards and 
          financial disclosure regulations.

Subparts B-D [Reserved]

    Authority: 5 U.S.C. 552a, 7301; 15 U.S.C. 2053(c).

    Source: 61 FR 65458, Dec. 13, 1996, unless otherwise noted.



                           Subpart A--General



Sec. 1030.101  Cross-references to employee ethical conduct standards and financial disclosure regulations.

    Employees of the Consumer Product Safety Commission are subject to 
the Standards of Ethical Conduct, 5 CFR part 2635, which are applicable 
to all executive branch personnel; the CPSC regulations at 5 CFR part 
8101, which supplement the executive branch standards; the Office of 
Personnel Management regulations on employee conduct at 5 CFR part 735; 
and the financial disclosure regulations at 5 CFR part 2634, which are 
applicable to all executive branch personnel. In addition, the 
Commissioners of the CPSC are subject to the statutory provisions of 15 
U.S.C. 2053(c).

Subparts B-D [Reserved]



PART 1031--COMMISSION PARTICIPATION AND COMMISSION EMPLOYEE INVOLVEMENT IN VOLUNTARY STANDARDS ACTIVITIES--Table of Contents




                       Subpart A--General Policies

Sec.
1031.1 Purpose and scope.
1031.2 Background.
1031.3 Consumer Product Safety Act amendments.
1031.4 Effect of voluntary standards activities on Commission 
          activities.
1031.5 Criteria for Commission participation in voluntary standards 
          activities.
1031.6 Extent and form of Commission involvement in the development of 
          voluntary standards.
1031.7 Commission support of voluntary standards activities.
1031.8 Voluntary Standards Coordinator.

                     Subpart B--Employee Involvement

1031.9 Purpose and scope.
1031.10 Definitions.
1031.11 Procedural safeguards.
1031.12 Membership criteria.
1031.13 Participation and monitoring criteria.
1031.14 Observation criteria.
1031.15 Communication criteria.

    Authority: 15 U.S.C. 2051-2083, 15 U.S.C. 1261-1276, 15 U.S.C. 1191-
1204.

    Source: 54 FR 6652, Feb. 14, 1989, unless otherwise noted.



                       Subpart A--General Policies



Sec. 1031.1  Purpose and scope.

    (a) This part 1031 sets forth the Consumer Product Safety 
Commission's guidelines and requirements on participating in the 
activities of voluntary standards bodies. Subpart A sets forth general 
policies on Commission participation, and subpart B sets forth policies 
and guidelines on employee involvement in voluntary standards 
activities.
    (b) For purposes of both subpart A and subpart B of this part 1031, 
voluntary standards bodies are private

[[Page 120]]

sector domestic or multinational organizations or groups, or 
combinations thereof, such as, but not limited to, all non-profit 
organizations, industry associations, professional and technical 
societies, institutes, and test laboratories, that are involved in the 
planning, development, establishment, revision, review or coordination 
of voluntary standards. Voluntary standards development bodies are 
voluntary standards bodies, or their sub-groups, that are devoted to 
developing or establishing voluntary standards.



Sec. 1031.2  Background.

    (a) Congress enacted the Consumer Product Safety Act in 1972 to 
protect consumers against unreasonable risks of injury associated with 
consumer products. In order to achieve that goal, Congress established 
the Consumer Product Safety Commission as an independent regulatory 
agency and granted it broad authority to promulgate mandatory safety 
standards for consumer products as a necessary alternative to industry 
self regulation.
    (b) In 1981, the Congress amended the Consumer Product Safety Act, 
The Federal Hazardous Substances Act, and the Flammable Fabrics Act, to 
require the Commission to rely on voluntary standards rather than 
promulgate a mandatory standard when voluntary standards would eliminate 
or adequately reduce the risk of injury addressed and it is likely that 
there will be substantial compliance with the voluntary standards. (15 
U.S.C. 2056(b), 15 U.S.C. 1262(g)(2), 15 U.S.C. 1193(h)(2)). The 1981 
Amendments also require the Commission, after any notice or advance 
notice of proposed rulemaking, to provide technical and administrative 
assistance to persons or groups who propose to develop or modify an 
appropriate voluntary standard. (15 U.S.C. 2054(a)(3)). Additionally, 
the amendments encourage the Commission to provide technical and 
administrative assistance to groups developing product safety standards 
and test methods, taking into account Commission resources and 
priorities (15 U.S.C. 2054(a)(4)). Although the Commission is required 
to provide assistance to such groups, it may determine the level of 
assistance in accordance with the level of its own administrative and 
technical resources and in accordance with its assessment of the 
likelihood that the groups being assisted will successfully develop a 
voluntary standard that will preclude the need for a mandatory standard.
    (c) In 1982, the Office of Management and Budget revised Circular 
No. A-119, Federal Participation in the Development and Use of Voluntary 
Standards. The Circular establishes the policy to be followed by 
executive agencies, including the Commission, in working with voluntary 
standards bodies and in adopting and using voluntary standards. The 
Circular encourages government participation in the standards-related 
activities of voluntary standards bodies and standards-developing groups 
when such participation is in the public interest and is compatible with 
the agencies, missions, authorities, priorities, and budget resources. 
The Circular recognizes, however, that voluntary standards activities, 
if improperly conducted, can suppress free and fair competition, impede 
innovation and technical progress, exclude safer and less expensive 
products, or otherwise adversely affect trade, commerce, health, or 
safety. Thus, agencies are urged to take full account of the impact on 
the economy, applicable Federal laws, policies and national objectives, 
including, for example, laws and regulations relating to antitrust, 
national security, small business, product safety, environment, 
technological development, and conflicts of interest.



Sec. 1031.3  Consumer Product Safety Act amendments.

    The Consumer Product Safety Act, as amended, contains several 
sections pertaining to the Commission's participation in the development 
and use of voluntary standards.
    (a) Section 7(b) provides that the Commission shall rely on 
voluntary consumer product safety standards prescribing requirements 
described in subsection (a) whenever compliance with such voluntary 
standards would eliminate or adequately reduce the risk of injury 
addressed and it is likely that there will be substantial compliance 
with such voluntary standards. (15 U.S.C. 2056(b)).

[[Page 121]]

    (b) Section 5(a)(3) provides that the Commission shall, following 
publication of an advance notice of proposed rulemaking or a notice of 
proposed rulemaking for a product safety rule under any rulemaking 
authority administered by the Commission, assist public and private 
organizations or groups of manufacturers, administratively and 
technically, in the development of safety standards addressing the risk 
of injury identified in such notice. (15 U.S.C. 2054(a)(3)).
    (c) Section 5(a)(4) provides that the Commission shall, to the 
extent practicable and appropriate (taking into account the resources 
and priorities of the Commission), assist public and private 
organizations or groups of manufacturers, administratively and 
technically, in the development of product safety standards and test 
methods. (15 U.S.C. 2054(a)(4)).



Sec. 1031.4  Effect of voluntary standards activities on Commission activities.

    (a)(1) The Commission, in determining whether to begin proceedings 
to develop mandatory standards under the acts it administers, considers 
whether mandatory regulation is necessary or whether there is an 
existing voluntary standard that adequately addresses the problem and 
the extent to which that voluntary standard is complied with by the 
affected industry.
    (2) The Commission acknowledges that there are situations in which 
adequate voluntary standards, in combination with appropriate 
certification programs, may be appropriate to support a conclusion that 
a mandatory standard is not necessary. The Commission may find that a 
mandatory standard is not necessary where compliance with an existing 
voluntary standard would eliminate or adequately reduce the risk of 
injury associated with the product, contains requirements and test 
methods that have been evaluated and found acceptable by the Commission, 
and it is likely that there will be substantial and timely compliance 
with the voluntary standard. Under such circumstances, the Commission 
may agree to encourage industry compliance with the voluntary standard 
and subsequently evaluate the effectiveness of the standard in terms of 
accident and injury reduction for products produced in compliance with 
the standard.
    (3) In evaluating voluntary standards, the Commission will relate 
the requirements of the standard to the identified risks of injury and 
evaluate the requirements in terms of their effectiveness in eliminating 
or reducing the risks of injury. The evaluation of voluntary standards 
will be conducted by Commission staff members, including representatives 
of legal, economics, engineering, epidemiological, health sciences, 
human factors, other appropriate interests, and the Voluntary Standards 
Coordinator. The staff evaluation will be conducted in a manner similar 
to evaluations of standards being considered for promulgation as 
mandatory standards.
    (4) In the event that the Commission has evaluated an existing 
voluntary standard and found it to be adequate in all but a few areas, 
the Commission may defer the initiation of a mandatory rulemaking 
proceeding and request the voluntary standards organization to revise 
the standard to address the identified inadequacies expeditiously. In 
such cases, the Commission may monitor or participate in the development 
of these revisions.
    (b) In the event the Commission determines that there is no existing 
voluntary standard that will eliminate or adequately reduce a risk of 
injury the Commission may commence a proceeding for the development of a 
consumer product safety rule or a regulation in accordance with section 
9 of the Consumer Product Safety Act, 15 U.S.C. 2058, section 3(f) of 
the Federal Hazardous Substances Act, 15 U.S.C. 1262(f), or section 4(a) 
of the Flammable Fabrics Act, 15 U.S.C. 1193(g), as may be applicable. 
In commencing such a proceeding, the Commission will publish an advance 
notice of proposed rulemaking which shall, among other things, invite 
any person to submit to the Commission an existing standard or portion 
of an existing standard, or to submit a statement of intention to modify 
or develop, within a reasonable period of time, a voluntary standard to 
address the risk of injury.
    (c) The Commission will consider those provisions of a voluntary 
standard that have been reviewed, evaluated,

[[Page 122]]

and deemed to be adequate in addressing the specified risks of injury 
when initiating a mandatory consumer product safety rule or regulation 
under the Consumer Product Safety Act, the Federal Hazardous Substances 
Act, or the Flammable Fabrics Act, as may be applicable. Comments will 
be requested in the advance notice of proposed rulemaking on the 
adequacy of such voluntary standard provisions.



Sec. 1031.5  Criteria for Commission participation in voluntary standards activities.

    The Commission will consider the extent to which the following 
criteria are met in considering Commission participation in the 
development of voluntary safety standards for consumer products:
    (a) The likelihood the voluntary standard will eliminate or 
adequately reduce the risk of injury addressed and that there will be 
substantial and timely compliance with the voluntary standard.
    (b) The likelihood that the voluntary standard will be developed 
within a reasonable period of time.
    (c) Exclusion, to the maximum extent possible, from the voluntary 
standard being developed, of requirements which will create 
anticompetitive effects or promote restraint of trade.
    (d) Provisions for periodic and timely review of the standard, 
including review for anticompetitive effects, and revision or amendment 
as the need arises.
    (e) Performance-oriented and not design-restrictive requirements, to 
the maximum practical extent, in any standard developed.
    (f) Industry arrangements for achieving substantial and timely 
industry compliance with the voluntary standard once it is issued, and 
the means of ascertaining such compliance based on overall market share 
of product production.
    (g) Provisions in the standard for marking products conforming to 
the standard so that future Commission investigation can indicate the 
involvement of such products in accidents and patterns of injury.
    (h) Provisions for insuring that products identified as conforming 
to such standards will be subjected to a testing and certification 
(including self-certification) procedure, which will provide assurance 
that the products comply with the standard.
    (i) The openness to all interested parties, and the establishment of 
procedures which will provide for meaningful participation in the 
development of such standards by representatives of producers, 
suppliers, distributors, retailers, consumers, small business, public 
interests and other individuals having knowledge or expertise in the 
areas under consideration, and procedures for affording other due 
process considerations.



Sec. 1031.6  Extent and form of Commission involvement in the development of voluntary standards.

    (a) The Commission shall approve agency ``participation'', as 
defined below, in the development and support of voluntary safety 
standards for consumer products. The Executive Director shall approve 
Commission activities that are defined below as ``monitoring.'' The 
extent of Commission involvement will be dependent upon the Commission's 
interest in the particular standards development activity and the 
commission's priorities and resources.
    (b) The Commission's interest in a specific voluntary standards 
activity will be based in part on the frequency and severity of injuries 
associated with the product, the involvement of the product in 
accidents, the susceptibility of the hazard to correction through 
standards, and the overall resources and priorities of the Commission. 
Commission involvement in voluntary standards activities generally will 
also be guided by the Commission's operating plan and budget.
    (c) There are two levels of Commission involvement in voluntary 
standards activities, each of which reflects a different level of 
Commission involvement as set forth below:
    (1) Monitoring. Monitoring involves maintaining an awareness of the 
voluntary standards development process

[[Page 123]]

through oral or written inquiries, receiving and reviewing minutes of 
meetings and copies of draft standards, or attending meetings for the 
purpose of observing and commenting during the standards development 
process in accordance with subpart B of this part. For example, 
monitoring may involve responding to requests from voluntary standards 
organizations, standards development committees, trade associations and 
consumer organizations; by providing information concerning the risks of 
injury associated with particular products, NEISS data, summaries and 
analyses of in-depth investigation reports; discussing Commission goals 
and objectives with regard to voluntary standards and improved consumer 
product safety; responding to requests for information concerning 
Commission programs; and initiating contacts with voluntary standards 
organizations to discuss cooperative voluntary standards activities.
    (2) Participating. Participating involves regularly attending 
meetings of a standard development committee or group and taking an 
active part in the discussions of the committee and in developing the 
standard, in accordance with subpart B of this part. Under certain 
conditions, the Commission will contribute to the deliberations of the 
committee by expending resources to provide technical assistance (e.g., 
research, engineering support, and information and education programs) 
and administrative assistance (e.g., travel costs, hosting meetings, and 
secretarial functions) which would support the development and 
implementation of voluntary standards. Participating may also include 
Commission support of voluntary standards activities as described in 
Sec. 1031.7.
    (d) Normally, the total amount of Commission support given to a 
voluntary standards activity shall be no greater than that of all non-
Federal participants in that activity, except where it is in the public 
interest to do so.
    (e) In the event of duplication of effort by two or more groups 
(either inside or outside the Commission) in developing a voluntary 
standard for the same product or class of products, the Commission shall 
encourage the several groups to cooperate in the development of a single 
voluntary standard.



Sec. 1031.7  Commission support of voluntary standards activities.

    (a) The Commission's support of voluntary safety standards 
development activities may include any one or a combination of the 
following actions:
    (1) Providing epidemiological and health science information and 
explanations of hazards for consumer products.
    (2) Encouraging the initiation of the development of voluntary 
standards for specific consumer products.
    (3) Identifying specific risks of injury to be addressed in a 
voluntary standard.
    (4) Performing or subsidizing technical assistance, including 
research, health science data, and engineering support, in the 
development of a voluntary standard activity in which the Commission is 
participating.
    (5) Providing assistance on methods of disseminating information and 
education about the voluntary standard or its use.
    (6) Performing a staff evaluation of a voluntary standard to 
determine its adequacy and efficacy in reducing the risks of injury that 
have been identified by the Commission as being associated with the use 
of the product.
    (7) Encouraging state and local governments to reference or 
incorporate the provisions of a voluntary standard in their regulations 
or ordinances and to participate in government or industrial model code 
development activities, so as to develop uniformity and minimize 
conflicting State and local regulations.
    (8) Monitoring the number and market share of products conforming to 
a voluntary safety standard.
    (9) Providing for the involvement of agency personnel in voluntary 
standards activities as described in subpart B of this part.
    (10) Providing administrative assistance, such as hosting meetings 
and secretarial assistance.
    (11) Providing funding support for voluntary standards development, 
as permitted by the agency budget.

[[Page 124]]

    (12) Taking other actions that the Commission believes appropriate 
in a particular situation.
    (b) [Reserved]



Sec. 1031.8  Voluntary Standards Coordinator.

    (a) The Executive Director shall appoint a Voluntary Standards 
Coordinator to coordinate agency participation in voluntary standards 
bodies so that:
    (1) The most effective use is made of agency personnel and 
resources, and
    (2) The views expressed by such personnel are in the public interest 
and, at a minimum, do not conflict with the interests and established 
views of the agency.
    (b) The Voluntary Standards Coordinator is responsible for managing 
the Commission's voluntary standards program, as well as preparing and 
submitting to the Commission a semiannual summary of its voluntary 
standards activities. The summary shall set forth, among other things, 
the goals of each voluntary standard under development, the extent of 
CPSC activity (monitoring or participation; the current status of 
standards development and implementation) and, if any, recommendations 
for additional Commission action. The Voluntary Standards Coordinator 
shall also compile information on the Commission's voluntary standards 
activities for the Commission's annual report.



                     Subpart B--Employee Involvement



Sec. 1031.9  Purpose and scope.

    (a) This subpart sets forth the Consumer Product Safety Commission's 
criteria and requirements governing membership and involvement by 
Commission officials and employees in the activities of voluntary 
standards development bodies.
    (b) The Commission realizes there are advantages and benefits 
afforded by greater involvement of Commission personnel in the standards 
activities of domestic and international voluntary standards 
organizations. However, such involvement might present an appearance or 
possibility of the Commission giving preferential treatment to an 
organization or group or of the Commission losing its independence or 
impartiality. Also, such participation may present real or apparent 
conflict of interest situations.
    (c) The purpose of this subpart is to further the objectives and 
programs of the Commission and to do so in a manner that ensures that 
such membership and participation:
    (1) Is consistent with the intent of the Consumer Product Safety Act 
and the other acts administered by the Commission, as well as with 
federal policy as set forth in the current version of OMB Circular No. 
A-119, Federal Participation in the Development and Use of Voluntary 
Standards;
    (2) Is not contrary to the public interest;
    (3) Presents no real or apparent conflict of interest, and does not 
result in or create the appearance of the Commission giving preferential 
treatment to an organization or group or the Commission compromising its 
independence or impartiality; and
    (4) Takes into account Commission resources and priorities.
    (d) In general, Commission employees must obtain approval from their 
supervisor and appropriate agency management to be involved in voluntary 
standards activities. They should also strive to apprise the Voluntary 
Standards Coordinator, where practicable, as to their involvement in 
voluntary standards activities.
    (e) All Commission employees involved in voluntary standards 
activities are subject to any restrictions for avoiding conflicts of 
interest and for avoiding situations that would present an appearance of 
bias.



Sec. 1031.10  Definitions.

    For purposes of describing the level of involvement in voluntary 
standards activities for which Commission employees may be authorized, 
the following definitions apply:
    (a) Membership. Membership is the status of an employee who joins a 
voluntary standards development or advisory organization or subgroup and 
is listed as a member. It includes all oral and written communications 
which are incidental to such membership.

[[Page 125]]

    (b) Participation. Participation is the active, ongoing involvement 
of an official or employee in the development of a new or revised 
voluntary standard pertaining to a particular consumer product or to a 
group of products that is the subject of a Commission hazard project. 
These projects should be one of those that are approved by the 
Commission, either by virtue of the agency's annual budget or operating 
plan, or by other specific agency authorization or decision, and are in 
accord with subpart A. Participation includes regularly attending 
meetings of a standards development committee or group, taking an active 
part in discussions and technical debates, registering opinions and 
expending other resources in support of a voluntary standard development 
activity. It includes all oral and written communications which are part 
of the participation process.
    (c) Monitoring. Monitoring is involvement by an official or employee 
in maintaining an awareness of the voluntary standards development 
process by attendance at meetings, receiving and reviewing minutes of 
standards development meetings and copies of draft standards, and 
commenting during the standards development process. It involves all 
oral and written communications which are part of the monitoring 
process. These monitoring activities must be related to general 
voluntary standards projects set forth in the agency's annual budget or 
operating plan or otherwise approved by the agency.
    (d) Observation. Observation is the attendance by an official or 
employee at a meeting of a voluntary standards development group for the 
purpose of observing and gathering information.
    (e) Communication. Communication is the oral or written contact by 
an official or employee with a representative or committee of a 
voluntary standards organization or advisory group.



Sec. 1031.11  Procedural safeguards.

    (a) Subject to the provisions of this subpart and budgetary and time 
constraints, Commission employees may be involved in voluntary standards 
activities that will further the objectives and programs of the 
Commission, are consistent with ongoing and anticipated Commission 
regulatory programs as set forth in the agency's operating plan, and are 
in accord with the Commission's policy statement on participation in 
voluntary standards activities set forth in subpart A of this part.
    (b) Commission employees who are involved in the development of a 
voluntary standard and who later participate in an official evaluation 
of that standard for the Commission shall describe in any information, 
oral or written, presented to the Commission, the extent of their 
involvement in the development of the standard. Any evaluation or 
recommendation for Commission actions by such employee shall strive to 
be as objective as possible and be reviewed by higher-level Commission 
officials or employees prior to submission to the Commission.
    (c) Involvement of a Commission official or employee in a voluntary 
standards committee shall be predicated on an understanding by the 
voluntary standards group that participation by Commission officials and 
employees is on a non-voting basis.
    (d) In no case shall Commission employees or officials vote or 
otherwise formally indicate approval or disapproval of a voluntary 
standard during the course of a voluntary standard development process.
    (e) Commission employees and officials who are involved in the 
development of voluntary standards may not accept voluntary standards 
committee leadership positions, e.g., committee chairman or secretary. 
Subject to prior approval by the Executive Director, a Commission 
employee or official may accept other committee positions only if it 
appears to be clearly in the public interest for the employee to carry 
out the functions of that specific position.
    (f) Attendance of Commission personnel at voluntary standards 
meetings shall be noted in the public calendar and meeting summaries 
shall be submitted to the Office of the Secretary as required by the 
Commission's meetings policy, 16 CFR part 1012.



Sec. 1031.12  Membership criteria.

    (a) The Commissioners, their special assistants, and Commission 
officials and employees holding the positions listed below, may not 
become members

[[Page 126]]

of a voluntary standards group because they either have the 
responsibility for making final decisions, or advise those who make 
final decisions, on whether to rely on a voluntary standard, promulgate 
a consumer product safety standard, or to take other action to prevent 
or reduce an unreasonable risk of injury associated with a product.
    (1) The Commissioners;
    (2) The Commissioners' Special Assistants;
    (3) The General Counsel and General Counsel Staff;
    (4) The Executive Director, the Deputy Executive Director, and 
special assistants to the Executive Director;
    (5) The Associate Executive Directors and Office Directors;
    (6) The Director of the Office of Program Management and Budget and 
any Special Assistants to the Director.
    (b) All other officials and employees not covered under 
Sec. 1031.12(a) may be advisory, non-voting members of voluntary 
standards development and advisory groups with the advance approval of 
the Executive Director. In particular, the Commission's Voluntary 
Standards Coordinator may accept such membership.
    (c) Commission employees or officials who have the approval of the 
Executive Director to accept membership in a voluntary standards 
organization or group pursuant to paragraph (b) of this section shall 
apprise the General Counsel and the Voluntary Standards Coordinator 
prior to their acceptance.
    (d) Commission officials or employees who desire to become a member 
of a voluntary standards body or group in their individual capacity must 
obtain prior approval of the Commission's Ethics Counselor for an 
outside activity pursuant to the Commission's Employee Standards of 
Conduct, 16 CFR part 1030.



Sec. 1031.13  Participation and monitoring criteria.

    (a) Commission officials, other than those positions listed in 
Sec. 1031.12(a), may participate in or monitor the development of 
voluntary safety standards for consumer products, but only in their 
official capacity as employees of the Commission and if permitted to do 
so by their supervisor and any other person designated by agency 
management procedures. Such participation or monitoring shall be in 
accordance with Commission procedures.
    (b) Employees in positions listed in Sec. 1031.12(a) (4), (5), and 
(6) may, on a case-by-case basis, participate in or monitor the 
development of a voluntary standard provided that they have the specific 
advance approval of the Commission.
    (c) Except in extraordinary circumstances and when approved in 
advance by the Executive Director in accordance with the provisions of 
the Commission's meetings policy, 16 CFR part 1012, Commission personnel 
shall not become involved in meetings concerning the development of 
voluntary standards that are not open to the public for attendance and 
observation. Attendance of Commission personnel at a voluntary standard 
meeting shall be noted in the public calendar and meeting logs filed 
with the Office of the Secretary in accordance with the Commission's 
meetings policy.
    (d) Generally, Commission employees may become involved in the 
development of voluntary standards only if they are made available for 
comment by all interested parties prior to their use or adoption.
    (e) Involvement by Commission officials and employees in voluntary 
standards bodies or standards-developing groups does not, of itself, 
connote Commission agreement with, or endorsement of, decisions reached, 
approved or published by such bodies or groups.



Sec. 1031.14  Observation criteria.

    A Commission official or employee may, on occasion, attend voluntary 
standards meetings for the sole purpose of observation, with the advance 
approval of his or her supervisor and any other person designated by 
agency management procedures. Commission officials and employees shall 
notify the Voluntary Standard Coordinator, for information purposes, 
prior to observing a voluntary standards meeting.



Sec. 1031.15  Communication criteria.

    (a) Commission officials and employees, who are not in the positions 
listed in Sec. 1031.12(a), or who are not already

[[Page 127]]

authorized to communicate with a voluntary standards group or 
representative incidental to their approved membership in a voluntary 
standard organization or group or as part of their participation or 
monitoring of a voluntary standard, may:
    (1) Communicate, within the scope of their duties, with a voluntary 
standard group, representative, or other committee member, on voluntary 
standards matters which are substantive in nature, i.e., matters that 
pertain to the formulation of the technical aspects of a specific 
voluntary standard or the course of conduct for developing the standard, 
only with the specific advance approval from the person or persons to 
whom they apply to obtain approval for participation or monitoring 
pursuant to Sec. 1031.13. The approval may indicate the duration of the 
approval and any other conditions.
    (2) Communicate, within the scope of their duties, with a voluntary 
standard group, representative, or other committee member, concerning 
voluntary standards activities which are not substantive in nature.
    (b) Commission employees may communicate with voluntary standards 
organizations only in accordance with Commission procedures.
    (c) Commissioners can engage in substantive and non-substantive 
written communications with voluntary standards bodies or 
representatives, provided a disclaimer in such communications indicates 
that any substantive views expressed are only their individual views and 
are not necessarily those of the Commission. Where a previous official 
Commission vote has taken place, that vote should also be noted in any 
such communication. Copies of such communications shall thereafter be 
provided to the other Commissioners, the Office of the Secretary, and 
the Voluntary Standards Coordinator.
    (d) The Voluntary Standards Coordinator shall be furnished a copy of 
each written communication of a substantive nature and a report of each 
oral communication of a substantive nature between a Commission official 
or employee and a voluntary standards organization or representative 
which pertains to a voluntary standards activity. The information shall 
be provided to the Voluntary Standards Coordinator as soon as 
practicable after the communication has taken place.



PART 1033--DISPLAY OF CONTROL NUMBERS FOR COLLECTION OF INFORMATION REQUIREMENTS UNDER THE PAPERWORK REDUCTION ACT--Table of Contents




Sec.
1033.1 Purpose.
1033.2 Display of control numbers.

    Authority: 44 U.S.C. 3506(c)(1); 5 U.S.C. 553.



Sec. 1033.1  Purpose.

    The purpose of this part 1033 is to display all control numbers 
assigned by the Office of Management and Budget (OMB) to collection of 
information requirements contained in rules enforced by the Consumer 
Product Safety Commission. Display of OMB control numbers is required by 
provisions of the Paperwork Reduction Act at 44 U.S.C. 3507(f) and by 
regulations issued by OMB to implement that act at 5 CFR 1320.7(f)(2), 
1320.12(d), 1320.13(j), and 1320.14(e).

[48 FR 57478, Dec. 30, 1983]



Sec. 1033.2  Display of control numbers.

    The following rules enforced by the Consumer Product Safety 
Commission containing collections of information are listed with the 
control numbers assigned by the Office of Management and Budget:

------------------------------------------------------------------------
                                                              Currently
                                                               assigned
  Part or section of title 16 Code of Federal Regulations    OMB control
                                                                 No.
------------------------------------------------------------------------
Part 1019..................................................    3041-0003
Part 1204..................................................    3041-0006
Part 1509..................................................    3041-0012
Part 1508..................................................    3041-0013
Part 1632..................................................    3041-0014
Part 1210..................................................    3041-0016
Part 1630, 1631............................................    3041-0017
Sections 1500.18(a)(6), 1500.86(a)(4)......................    3041-0019
Part 1209..................................................    3041-0022
Parts 1610, 1611...........................................    3041-0024
Parts 1615, 1616...........................................    3041-0027
Part 1505..................................................    3041-0035
Part 1406..................................................    3041-0040
Part 1205..................................................    3041-0091
Part 1211..................................................    3041-0125
------------------------------------------------------------------------


(44 U.S.C. 3506(c)(1); 5 U.S.C. 553)

[62 FR 42397, Aug. 7, 1997]

[[Page 128]]



PART 1034--ENFORCEMENT OF NONDISCRIMINATION ON THE BASIS OF HANDICAP IN PROGRAMS OR ACTIVITIES CONDUCTED BY THE CONSUMER PRODUCT SAFETY COMMISSION--Table of Contents




Sec.
1034.101 Purpose.
1034.102 Application.
1034.103 Definitions.
1034.104-1034.109 [Reserved]
1034.110 Self-evaluation.
1034.111 Notice.
1034.112-1034.129 [Reserved]
1034.130 General prohibitions against discrimination.
1034.131-1034.139 [Reserved]
1034.140 Employment.
1034.141-1034.148 [Reserved]
1034.149 Program accessibility: Discrimination prohibited.
1034.150 Program accessibility: Existing facilities.
1034.151 Program accessibility: New construction and alterations.
1034.152-1034.159 [Reserved]
1034.160 Communications.
1034.161-1034.169 [Reserved]
1034.170 Compliance procedures.
1034.171-1034.999 [Reserved]

    Authority: 29 U.S.C. 794.

    Source: 51 FR 4575, 4579, Feb. 5, 1986; 52 FR 405, Jan. 6, 1987, 
unless otherwise noted.



Sec. 1034.101  Purpose.

    This part effectuates section 119 of the Rehabilitation, 
Comprehensive Services, and Developmental Disabilities Amendments of 
1978, which amended section 504 of the Rehabilitation Act of 1973 to 
prohibit discrimination on the basis of handicap in programs or 
activities conducted by Executive agencies or the United States Postal 
Service.



Sec. 1034.102  Application.

    This part applies to all programs or activities conducted by the 
agency.



Sec. 1034.103  Definitions.

    For purposes of this part, the term--
    Assistant Attorney General means the Assistant Attorney General, 
Civil Rights Division, United States Department of Justice.
    Auxiliary aids means services or devices that enable persons with 
impaired sensory, manual, or speaking skills to have an equal 
opportunity to participate in, and enjoy the benefits of, programs or 
activities conducted by the agency. For example, auxiliary aids useful 
for persons with impaired vision include readers, Brailled materials, 
audio recordings, telecommunications devices and other similar services 
and devices. Auxiliary aids useful for persons with impaired hearing 
include telephone handset amplifiers, telephones compatible with hearing 
aids, telecommunication devices for deaf persons (TDD's), interpreters, 
notetakers, written materials, and other similar services and devices.
    Complete complaint means a written statement that contains the 
complainant's name and address and describes the agency's alleged 
discriminatory action in sufficient detail to inform the agency of the 
nature and date of the alleged violation of section 504. It shall be 
signed by the complainant or by someone authorized to do so on his or 
her behalf. Complaints filed on behalf of classes or third parties shall 
describe or identify (by name, if possible) the alleged victims of 
discrimination.
    Facility means all or any portion of buildings, structures, 
equipment, roads, walks, parking lots, rolling stock or other 
conveyances, or other real or personal property.
    Handicapped person means any person who has a physical or mental 
impairment that substantially limits one or more major life activities, 
has a record of such an impairment, or is regarded as having such an 
impairment.
    As used in this definition, the phrase:
    (1) Physical or mental impairment includes--
    (i) Any physiological disorder or condition, cosmetic disfigurement, 
or anatomical loss affecting one of more of the following body systems: 
Neurological; musculoskeletal; special sense organs; respiratory, 
including speech organs; cardiovascular; reproductive; digestive; 
genitourinary; hemic and lymphatic; skin; and endocrine; or
    (ii) Any mental or psychological disorder, such as mental 
retardation, organic brain syndrome, emotional or mental illness, and 
specific learning disabilities. The term physical or mental impairment 
includes, but is not limited

[[Page 129]]

to, such diseases and conditions as orthopedic, visual, speech, and 
hearing impairments, cerebral palsy, epilepsy, muscular dystrophy, 
multiple sclerosis, cancer, heart disease, diabetes, mental retardation, 
emotional illness, and drug addition and alcholism.
    (2) Major life activities includes functions such as caring for 
one's self, performing manual tasks, walking, seeing, hearing, speaking, 
breathing, learning, and working.
    (3) Has a record of such an impairment means has a history of, or 
has been misclassified as having, a mental or physical impairment that 
substantially limits one or more major life activities.
    (4) Is regarded as having an impairment means--
    (i) Has a physical or mental impairment that does not substantially 
limit major life activities but is treated by the agency as constituting 
such a limitation;
    (ii) Has a physical or mental impairment that substantially limits 
major life activities only as a result of the attitudes of others toward 
such impairment; or
    (iii) Has none of the impairments defined in subparagraph (1) of 
this definition but is treated by the agency as having such an 
impairment.
    Qualified handicapped person means--
    (1) With respect to any agency program or activity under which a 
person is required to perform services or to achieve a level of 
accomplishment, a handicapped person who meets the essential eligibility 
requirements and who can achieve the purpose of the program or activity 
without modifications in the program or activity that the agency can 
demonstrate would result in a fundamental alteration in its nature; or
    (2) With respect to any other program or activity, a handicapped 
person who meets the essential eligibility requirements for 
participation in, or receipt of benefits from, that program or activity.
    (3) Qualified handicapped person is defined for purposes of 
employment in 29 CFR 1613.702(f), which is made applicable to this part 
by Sec. 1034.140.
    Section 504 means section 504 of the Rehabilitation Act of 1973 
(Pub. L. 93-112, 87 Stat. 394 (29 U.S.C. 794)), as amended by the 
Rehabilitation Act Amendments of 1974 (Pub. L. 93-516, 88 Stat. 1617), 
and the Rehabilitation, Comprehensive Services, and Developmental 
Disabilities Amendments of 1978 (Pub. L. 95-602, 92 Stat. 2955). As used 
in this part, section 504 applies only to programs or activities 
conducted by Executive agencies and not to federally assisted programs.

[51 FR 4575, 4579, Feb. 5, 1986; 51 FR 7543, Mar. 5, 1986]



Sec. Sec. 1034.104-1034.109  [Reserved]



Sec. 1034.110  Self-evaluation.

    (a) The agency shall, by April 9, 1987, evaluate its current 
policies and practices, and the effects thereof, that do not or may not 
meet the requirements of this part, and, to the extent modification of 
any such policies and practices is required, the agency shall proceed to 
make the necessary modifications.
    (b) The agency shall provide an opportunity to interested persons, 
including handicapped persons or organizations representing handicapped 
persons, to participate in the self-evaluation process by submitting 
comments (both oral and written).
    (c) The agency shall, until three years following the completion of 
the self-evaluation, maintain on file and make available for public 
inspections:
    (1) A description of areas examined and any problems identified, and
    (2) A description of any modifications made.



Sec. 1034.111  Notice.

    The agency shall make available to employees, applicants, 
participants, beneficiaries, and other interested persons such 
information regarding the provisions of this part and its applicability 
to the programs or activities conducted by the agency, and make such 
information available to them in such manner as the head of the agency 
finds necessary to apprise such persons of the protections against 
discrimination assured them by section 504 and this regulation.

[[Page 130]]



Sec. Sec. 1034.112-1034.129  [Reserved]



Sec. 1034.130  General prohibitions against discrimination.

    (a) No qualified handicapped person shall, on the basis of handicap, 
be excluded from participation in, be denied the benefits of, or 
otherwise be subjected to discrimination under any program or activity 
conducted by the agency.
    (b)(1) The agency, in providing any aid, benefit, or service, may 
not, directly or through contractual, licensing, or other arrangements, 
on the basis of handicap--
    (i) Deny a qualified handicapped person the opportunity to 
participate in or benefit from the aid, benefit, or service;
    (ii) Afford a qualified handicapped person an opportunity to 
participate in or benefit from the aid, benefit, or service that is not 
equal to that afforded others;
    (iii) Provide a qualified handicapped person with an aid, benefit, 
or service that is not as effective in affording equal opportunity to 
obtain the same result, to gain the same benefit, or to reach the same 
level of achievement as that provided to others;
    (iv) Provide different or separate aid, benefits, or services to 
handicapped persons or to any class of handicapped persons than is 
provided to others unless such action is necessary to provide qualified 
handicapped persons with aid, benefits, or services that are as 
effective as those provided to others;
    (v) Deny a qualified handicapped person the opportunity to 
participate as a member of planning or advisory boards; or
    (vi) Otherwise limit a qualified handicapped person in the enjoyment 
of any right, privilege, advantage, or opportunity enjoyed by others 
receiving the aid, benefit, or service.
    (2) The agency may not deny a qualified handicapped person the 
opportunity to participate in programs or activities that are not 
separate or different, despite the existence of permissibly separate or 
different programs or activities.
    (3) The agency may not, directly or through contractual or other 
arrangements, utilize criteria or methods of administration the purpose 
or effect of which would--
    (i) Subject qualified handicapped persons to discrimination on the 
basis of handicap; or
    (ii) Defeat or substantially impair accomplishment of the objectives 
of a program or activity with respect to handicapped persons.
    (4) The agency may not, in determining the site or location of a 
facility, make selections the purpose or effect of which would--
    (i) Exclude handicapped persons from, deny them the benefits of, or 
otherwise subject them to discrimination under any program or activity 
conducted by the agency; or
    (ii) Defeat or substantially impair the accomplishment of the 
objectives of a program or activity with respect to handicapped persons.
    (5) The agency, in the selection of procurement contractors, may not 
use criteria that subject qualified handicapped persons to 
discrimination on the basis of handicap.
    (c) The exclusion of nonhandicapped persons from the benefits of a 
program limited by Federal statute or Executive order to handicapped 
persons or the exclusion of a specific class of handicapped persons from 
a program limited by Federal statute or Executive order to a different 
class of handicapped persons is not prohibited by this part.
    (d) The agency shall administer programs and activities in the most 
integrated setting appropriate to the needs of qualified handicapped 
persons.



Sec. Sec. 1034.131-1034.139  [Reserved]



Sec. 1034.140  Employment.

    No qualified handicapped person shall, on the basis of handicap, be 
subjected to discrimination in employment under any program or activity 
conducted by the agency. The definitions, requirements, and procedures 
of section 501 of the Rehabilitation Act of 1973 (29 U.S.C. 791), as 
established by the Equal Employment Opportunity Commission in 29 CFR 
part 1613, shall apply to employment in federally conducted programs or 
activities.

[[Page 131]]



Sec. Sec. 1034.141-1034.148  [Reserved]



Sec. 1034.149  Program accessibility: Discrimination prohibited.

    Except as otherwise provided in Sec. 1034.150, no qualified 
handicapped person shall, because the agency's facilities are 
inaccessible to or unusable by handicapped persons, be denied the 
benefits of, be excluded from participation in, or otherwise be 
subjected to discrimination under any program or activity conducted by 
the agency.



Sec. 1034.150  Program accessibility: Existing facilities.

    (a) General. The agency shall operate each program or activity so 
that the program or activity, when viewed in its entirety, is readily 
accessible to and usable by handicapped persons. This paragraph does 
not--
    (1) Necessarily require the agency to make each of its existing 
facilities accessible to and usable by handicapped persons; or
    (2) Require the agency to take any action that it can demonstrate 
would result in a fundamental alteration in the nature of a program or 
activity or in undue financial and administrative burdens. In those 
circumstances where agency personnel believe that the proposed action 
would fundamentally alter the program or activity or would result in 
undue financial and administrative burdens, the agency has the burden of 
proving that compliance with Sec. 1034.150(a) would result in such 
alteration or burdens. The decision that compliance would result in such 
alteration or burdens must be made by the agency head or his or her 
designee after considering all agency resources available for use in the 
funding and operation of the conducted program or activity, and must be 
accompanied by a written statement of the reasons for reaching that 
conclusion. If an action would result in such an alteration or such 
burdens, the agency shall take any other action that would not result in 
such an alteration or such burdens but would nevertheless ensure that 
handicapped persons receive the benefits and services of the program or 
activity.
    (b) Methods. The agency may comply with the requirements of this 
section through such means as redesign of equipment, reassignment of 
services to accessible buildings, assignment of aides to beneficiaries, 
home visits, delivery of services at alternate accessible sites, 
alteration of existing facilities and construction of new facilities, 
use of accessible rolling stock, or any other methods that result in 
making its programs or activities readily accessible to and usable by 
handicapped persons. The agency is not required to make structural 
changes in existing facilities where other methods are effective in 
achieving compliance with this section. The agency, in making 
alterations to existing buildings, shall meet accessibility requirements 
to the extent compelled by the Architectural Barriers Act of 1968, as 
amended (42 U.S.C. 4151-4157), and any regulations implementing it. In 
choosing among available methods for meeting the requirements of this 
section, the agency shall give priority to those methods that offer 
programs and activities to qualified handicapped persons in the most 
integrated setting appropriate.
    (c) Time period for compliance. The agency shall comply with the 
obligations established under this section by June 6, 1986, except that 
where structural changes in facilities are undertaken, such changes 
shall be made by April 7, 1989, but in any event as expeditiously as 
possible.
    (d) Transition plan. In the event that structural changes to 
facilities will be undertaken to achieve program accessibility, the 
agency shall develop, by October 7, 1986, a transition plan setting 
forth the steps necessary to complete such changes. The agency shall 
provide an opportunity to interested persons, including handicapped 
persons or organizations representing handicapped persons, to 
participate in the development of the transition plan by submitting 
comments (both oral and written). A copy of the transition plan shall be 
made available for public inspection. The plan shall, at a minimum--
    (1) Identify physical obstacles in the agency's facilities that 
limit the accessibility of its programs or activities to handicapped 
persons;

[[Page 132]]

    (2) Describe in detail the methods that will be used to make the 
facilities accessible;
    (3) Specify the schedule for taking the steps necessary to achieve 
compliance with this section and, if the time period of the transition 
plan is longer than one year, identify steps that will be taken during 
each year of the transition period; and
    (4) Indicate the official responsible for implementation of the 
plan.

[51 FR 4575, 4579, Feb. 5, 1986; 51 FR 7543, Mar. 5, 1986]



Sec. 1034.151  Program accessibility: New construction and alterations.

    Each building or part of a building that is constructed or altered 
by, on behalf of, or for the use of the agency shall be designed, 
constructed, or altered so as to be readily accessible to and usable by 
handicapped persons. The definitions, requirements, and standards of the 
Architectural Barriers Act (42 U.S.C. 4151-4157), as established in 41 
CFR 101-19.600 to 101-19.607, apply to buildings covered by this 
section.



Sec. Sec. 1034.152-1034.159  [Reserved]



Sec. 1034.160  Communications.

    (a) The agency shall take appropriate steps to ensure effective 
communication with applicants, participants, personnel of other Federal 
entities, and members of the public.
    (1) The agency shall furnish appropriate auxiliary aids where 
necessary to afford a handicapped person an equal opportunity to 
participate in, and enjoy the benefits of, a program or activity 
conducted by the agency.
    (i) In determining what type of auxiliary aid is necessary, the 
agency shall give primary consideration to the requests of the 
handicapped person.
    (ii) The agency need not provide individually prescribed devices, 
readers for personal use or study, or other devices of a personal 
nature.
    (2) Where the agency communicates with applicants and beneficiaries 
by telephone, telecommunication devices for deaf persons (TDD's) or 
equally effective telecommunication systems shall be used.
    (b) The agency shall ensure that interested persons, including 
persons with impaired vision or hearing, can obtain information as to 
the existence and location of accessible services, activities, and 
facilities.
    (c) The agency shall provide signage at a primary entrance to each 
of its inaccessible facilities, directing users to a location at which 
they can obtain information about accessible facilities. The 
international symbol for accessibility shall be used at each primary 
entrance of an accessible facility.
    (d) This section does not require the agency to take any action that 
it can demonstrate would result in a fundamental alteration in the 
nature of a program or activity or in undue financial and administrative 
burdens. In those circumstances where agency personnel believe that the 
proposed action would fundamentally alter the program or activity or 
would result in undue financial and administrative burdens, the agency 
has the burden of proving that compliance with Sec. 1034.160 would 
result in such alteration or burdens. The decision that compliance would 
result in such alteration or burdens must be made by the agency head or 
his or her designee after considering all agency resources available for 
use in the funding and operation of the conducted program or activity, 
and must be accompanied by a written statement of the reasons for 
reaching that conclusion. If an action required to comply with this 
section would result in such an alteration or such burdens, the agency 
shall take any other action that would not result in such an alteration 
or such burdens but would nevertheless ensure that, to the maximum 
extent possible, handicapped persons receive the benefits and services 
of the program or activity.



Sec. Sec. 1034.161-1034.169  [Reserved]



Sec. 1034.170  Compliance procedures.

    (a) Except as provided in paragraph (b) of this section, this 
section applies to all allegations of discrimination on the basis of 
handicap in programs or activities conducted by the agency.
    (b) The agency shall process complaints alleging violations of 
section 504 with respect to employment according to the procedures 
established by the Equal Employment Opportunity

[[Page 133]]

Commission in 29 CFR part 1613 pursuant to section 501 of the 
Rehabilitation Act of 1973 (29 U.S.C. 791).
    (c) The Office of Equal Employment Opportunity and Minority 
Enterprise shall be responsible for coordinating implementation of this 
section. Complaints may be sent to the Director, Office of Equal 
Employment Opportunity and Minority Enterprise, Consumer Product Safety 
Commission, Washington, D.C. 20207.
    (d) The agency shall accept and investigate all complete complaints 
for which it has jurisdiction. All complete complaints must be filed 
within 180 days of the alleged act of discrimination. The agency may 
extend this time period for good cause.
    (e) If the agency receives a complaint over which it does not have 
jurisdiction, it shall promptly notify the complainant and shall make 
reasonable efforts to refer the complaint to the appropriate government 
entity.
    (f) The agency shall notify the Architectural and Transportation 
Barriers Compliance Board upon receipt of any complaint alleging that a 
building or facility that is subject to the Architectural Barriers Act 
of 1968, as amended (42 U.S.C. 4151-4157), or section 502 of the 
Rehabilitation Act of 1973, as amended (29 U.S.C. 792), is not readily 
accessible to and usable by handicapped persons.
    (g) Within 180 days of the receipt of a complete complaint for which 
it has jurisdiction, the agency shall notify the complainant of the 
results of the investigation in a letter containing--
    (1) Findings of fact and conclusions of law;
    (2) A description of a remedy for each violation found; and
    (3) A notice of the right to appeal.
    (h) Appeals of the findings of fact and conclusions of law or 
remedies must be filed by the complainant within 90 days of receipt from 
the agency of the letter required by Sec. 1034.170(g). The agency may 
extend this time for good cause.
    (i) Timely appeals shall be accepted and processed by the head of 
the agency.
    (j) The head of the agency shall notify the complainant of the 
results of the appeal within 60 days of the receipt of the request. If 
the head of the agency determines that additional information is needed 
from the complainant, he or she shall have 60 days from the date of 
receipt of the additional information to make his or her determination 
on the appeal.
    (k) The time limits cited in paragraphs (g) and (j) of this section 
may be extended with the permission of the Assistant Attorney General.
    (l) The agency may delegate its authority for conducting complaint 
investigations to other Federal agencies, except that the authority for 
making the final determination may not be delegated to another agency.

[51 FR 4575, 4579, Feb. 5, 1986, as amended at 51 FR 4575, Feb. 5, 1986]



Sec. Sec. 1034.171-1034.999  [Reserved]



PART 1051--PROCEDURE FOR PETITIONING FOR RULEMAKING--Table of Contents




Sec.
1051.1 Scope.
1051.2 General.
1051.3 Place of filing.
1051.4 Time of filing.
1051.5 Requirements and recommendations for petitions.
1051.6 Documents not considered petitions.
1051.7 Statement in support of or in opposition to petitions; Duty of 
          petitioners to remain apprised of developments regarding 
          petitions.
1051.8 Public hearings on petitions.
1051.9 Factors the Commission considers in granting or denying 
          petitions.
1051.10 Granting petitions.
1051.11 Denial of petitions.

    Authority: 5 U.S.C. 553(e), 5 U.S.C. 555(e).

    Source: 48 FR 57123, Dec. 28, 1983, unless otherwise noted.



Sec. 1051.1  Scope.

    (a) This part establishes procedures for the submission and 
disposition of petitions for the issuance, amendment or revocation of 
rules under the Consumer Product Safety Act (CPSA) (15 U.S.C. 2051 et 
seq.) or other statutes administered by the Consumer Product Safety 
Commission.
    (b) Persons filing petitions for rulemaking shall follow as closely 
as possible the requirements and are encouraged to follow as closely as 
possible the recommendations for filing petitions under Sec. 1051.5.

[[Page 134]]

    (c) Petitions regarding products regulated under the Federal 
Hazardous Substances Act (FHSA) (15 U.S.C. 1261 et seq.) are governed by 
existing Commission procedures at 16 CFR 1500.82. Petitions regarding 
the exemption of products regulated under the Poison Prevention 
Packaging Act of 1970 (PPPA) (15 U.S.C. 1471 et seq.) are governed by 
existing Commission procedures at 16 CFR part 1702. In addition, 
however, persons filing such petitions shall follow the requirements and 
are encouraged to follow the recommendations for filing petitions as set 
forth in Sec. 1051.5.

[48 FR 57123, Dec. 28, 1983 as amended at 64 FR 48704, Sept. 8, 1999]



Sec. 1051.2  General.

    (a) Any person may file with the Commission a petition requesting 
the Commission to begin a proceeding to issue, amend or revoke a 
regulation under any of the statutes it administers.
    (b) A petition which addresses a risk of injury associated with a 
product which could be eliminated or reduced to a sufficient extent by 
action taken under the Federal Hazardous Substances Act, the Poison 
Prevention Packaging Act of 1970, or the Flammable Fabrics Act may be 
considered by the Commission under those Acts. However, if the 
Commission finds by rule, in accordance with section 30(d) of the CPSA, 
as amended by Public Law 94-284, that it is in the public interest to 
regulate such risk of injury under the CPSA, it may do so. Upon 
determination by the Office of the General Counsel that a petition 
should be considered under one of these acts rather than the CPSA, the 
Office of the Secretary shall docket and process the petition under the 
appropriate act and inform the petitioner of this determination. Such 
docketing, however, shall not preclude the Commission from proceeding to 
regulate the product under the CPSA after making the necessary findings.



Sec. 1051.3  Place of filing.

    A petition should be mailed to: Office of the Secretary, Consumer 
Product Safety Commission, Washington, DC 20207. Persons wishing to file 
a petition in person may do so in the Office of the Secretary, at 4330 
East West Highway, Bethesda, Maryland.

[48 FR 57123, Dec. 28, 1983, as amended at 62 FR 46667, Sept. 4, 1997]



Sec. 1051.4  Time of filing.

    For purposes of computing time periods under this part, a petition 
shall be considered filed when time-date stamped by the Office of the 
Secretary. A document is time-date stamped when it is received in the 
Office of the Secretary.



Sec. 1051.5  Requirements and recommendations for petitions.

    (a) Requirements. To be considered a petition under this part, any 
request to issue, amend or revoke a rule shall meet the requirements of 
this paragraph (a). A petition shall:
    (1) Be written in the English language;
    (2) Contain the name and address of the petitioner;
    (3) Indicate the product (or products) regulated under the Consumer 
Product Safety Act or other statute the Commission administers for which 
a rule is sought or for which there is an existing rule sought to be 
modified or revoked. (If the petition regards a procedural or other rule 
not involving a specific product, the type of rule involved must be 
indicated.)
    (4) Set forth facts which establish the claim that the issuance, 
amendment, or revocation of the rule is necessary (for example, such 
facts may include personal experience; medical, engineering or injury 
data; or a research study); and
    (5) Contain an explicit request to initiate Commission rulemaking 
and set forth a brief description of the substance of the proposed rule 
or amendment or revocation thereof which it is claimed should be issued 
by the Commission. (A general request for regulatory action which does 
not reasonably specify the type of action requested shall not be 
sufficient for purposes of this subsection.)
    (b) Recommendations. The Commission encourages the submission of as 
much information as possible related to the petition. Thus, to assist 
the Commission in its evaluation of a petition, to

[[Page 135]]

the extent the information is known and available to the petitioner, the 
petitioner is encouraged to supply the following information or any 
other information relating to the petition. The petition will be 
considered by the Commission even if the petitioner is unable to supply 
the information recommended in this paragraph (b). However, as 
applicable, and to the extent possible, the petitioner is encouraged to:
    (1) Describe the specific risk(s) of injury to which the petition is 
addressed, including the degree (severity) and the nature of the risk(s) 
of injury associated with the product and possible reasons for the 
existence of the risk of injury (for example, product defect, poor 
design, faulty workmanship, or intentional or unintentional misuse);
    (2) State why a consumer product safety standard would not be 
feasible if the petition requests the issuance of a rule declaring the 
product to be a banned hazardous product; and
    (3) Supply or reference any known documentation, engineering 
studies, technical studies, reports of injuries, medical findings, legal 
analyses, economic analyses and environmental impact analyses relating 
to the petition.
    (c) Procedural recommendations. The following are procedural 
recommendations to help the Commission in its consideration of 
petitions. The Commission requests, but does not require, that a 
petition filed under this part:
    (1) Be typewritten,
    (2) Include the word ``petition'' in a heading preceding the text,
    (3) Specify what section of the statute administered by the 
Commission authorizes the requested rulemaking,
    (4) Include the telephone number of the petitioner, and
    (5) Be accompanied by at least five (5) copies of the petition.



Sec. 1051.6  Documents not considered petitions.

    (a) A document filed with the Commission which addresses a topic or 
involves a product outside the jurisdiction of the Commission will not 
be considered to be a petition. After consultation with the Office of 
the General Counsel, the Office of the Secretary, if appropriate, will 
forward to the appropriate agency documents which address products or 
topics within the jurisdiction of other agencies. The Office of the 
Secretary shall notify the sender of the document that it has been 
forwarded to the appropriate agency.
    (b) Any other documents filed with the Office of the Secretary that 
are determined by the Office of the General Counsel not to be petitions 
shall be evaluated for possible staff action. The Office of the General 
Counsel shall notify the writer of the manner in which the Commission 
staff is treating the document. If the writer has indicated an intention 
to petition the Commission, the Office of the General Counsel shall 
inform the writer of the procedure to be followed for petitioning.



Sec. 1051.7  Statement in support of or in opposition to petitions; Duty of petitioners to remain apprised of developments regarding petitions.

    (a) Any person may file a statement with the Office of the Secretary 
in support of or in opposition to a petition prior to Commission action 
on the petition. Persons submitting statements in opposition to a 
petition are encouraged to provide copies of such statements to the 
petitioner.
    (b) It is the duty of the petitioner, or any person submitting a 
statement in support of or in opposition to a petition, to keep himself 
or herself apprised of developments regarding the petition. Information 
regarding the status of petitions is available from the Office of the 
Secretary of the Commission.
    (c) The Office of the Secretary shall send to the petitioner a copy 
of the staff briefing package on his or her petition at the same time 
the package is transmitted to the Commissioners for decision.



Sec. 1051.8  Public hearings on petitions.

    (a) The Commission may hold a public hearing or may conduct such 
investigation or proceeding, including a public meeting, as it deems 
appropriate to determine whether a petition should be granted.
    (b) If the Commission decides that a public hearing on a petition, 
or any portion thereof, would contribute to its determination of whether 
to grant or

[[Page 136]]

deny the petition, it shall publish in the Federal Register a notice of 
a hearing on the petition and invite interested persons to submit their 
views through an oral or written presentation or both. The hearings 
shall be informal, nonadversary, legislative-type proceedings in 
accordance with 16 CFR part 1052.



Sec. 1051.9  Factors the Commission considers in granting or denying petitions.

    (a) The major factors the Commission considers in deciding whether 
to grant or deny a petition regarding a product include the following 
items:
    (1) Whether the product involved presents an unreasonable risk of 
injury.
    (2) Whether a rule is reasonably necessary to eliminate or reduce 
the risk of injury.
    (3) Whether failure of the Commission to initiate the rulemaking 
proceeding requested would unreasonably expose the petitioner or other 
consumers to the risk of injury which the petitioner alleges is 
presented by the product.
    (4) Whether, in the case of a petition to declare a consumer product 
a ``banned hazardous product'' under section 8 of the CPSA, the product 
is being or will be distributed in commerce and whether a feasible 
consumer product safety standard would adequately protect the public 
from the unreasonable risk of injury associated with such product.
    (b) In considering these factors, the Commission will treat as an 
important component of each one the relative priority of the risk of 
injury associated with the product about which the petition has been 
filed and the Commission's resources available for rulemaking activities 
with respect to that risk of injury. The CPSC Policy on Establishing 
Priorities for Commission Action, 16 CFR 1009.8, sets forth the criteria 
upon which Commission priorities are based.



Sec. 1051.10  Granting petitions.

    (a) The Commission shall either grant or deny a petition within a 
reasonable time after it is filed, taking into account the resources 
available for processing the petition. The Commission may also grant a 
petition in part or deny it in part. If the Commission grants a 
petition, it shall begin proceedings to issue, amend or revoke the rule 
under the appropriate provisions of the statutes under its 
administration. Beginning a proceeding means taking the first step in 
the rulemaking process (issuance of an advance notice of proposed 
rulemaking or a notice of proposed rulemaking, whichever is applicable).
    (b) Granting a petition and beginning a proceeding does not 
necessarily mean that the Commission will issue, amend or revoke the 
rule as requested in the petition. The Commission must make a final 
decision as to the issuance, amendment, or revocation of a rule on the 
basis of all available relevant information developed in the course of 
the rulemaking proceeding. Should later information indicate that the 
action is unwarranted or not necessary, the Commission may terminate the 
proceeding.



Sec. 1051.11  Denial of petitions.

    (a) If the Commission denies a petition it shall promptly notify the 
petitioner in writing of its reasons for such denial as required by the 
Administrative Procedure Act, 5 U.S.C. 555(e).
    (b) If the Commission denies a petition, the petitioner (or another 
party) can refile the petition if the party can demonstrate that new or 
changed circumstances or additional information justify reconsideration 
by the Commission.
    (c) A Commission denial of a petition shall not preclude the 
Commission from continuing to consider matters raised in the petition.



PART 1052--PROCEDURAL REGULATIONS FOR INFORMAL ORAL PRESENTATIONS IN PROCEEDINGS BEFORE THE CONSUMER PRODUCT SAFETY COMMISSION--Table of Contents




Sec.
1052.1 Scope and purpose.
1052.2 Notice of opportunity for oral presentation.
1052.3 Conduct of oral presentation.
1052.4 Presiding officer; appointment, duties, powers.


[[Page 137]]


    Authority: 15 U.S.C. 1193(d), 15 U.S.C. 2058(d)(2), 15 U.S.C. 
2076(a), and 5 U.S.C. 553(c).

    Source: 48 FR 57122, Dec. 28, 1983, unless otherwise noted.



Sec. 1052.1  Scope and purpose.

    (a) Section 9(d)(2) of the Consumer Product Safety Act, 15 U.S.C. 
2058(d)(2), and section 4(d) of the Flammable Fabrics Act, 15 U.S.C. 
1193(d), provide that certain rules under those statutes shall be 
promulgated pursuant to section 4 of the Administrative Procedure Act, 5 
U.S.C. 553, except that the Commission shall give interested persons an 
opportunity for the oral presentation of data, views or arguments in 
addition to the opportunity to make written submissions. Several 
rulemaking provisions of the statutes administered by the Commission are 
subject only to the rulemaking procedures of the Administrative 
Procedure Act. Section 4(c) of the Administrative Procedure Act provides 
that the opportunity for oral presentations may or may not be granted in 
rulemaking under that section. In addition, section 27(a) of the 
Consumer Product Safety Act, 15 U.S.C. 2076(a), authorizes informal 
proceedings that can be conducted in non-rulemaking investigatory 
situations.
    (b) This part sets forth rules of procedure for the oral 
presentation of data, views or arguments in the informal rulemaking or 
investigatory situations described in subsection (a) of this section. In 
situations where the opportunity for an oral presentation is not 
required by statute, the Commission will determine whether to provide 
the opportunity on a case-by-case basis.



Sec. 1052.2  Notice of opportunity for oral presentation.

    The Commission will publish in the Federal Register notice of 
opportunity for an oral presentation in each instance. The notice shall 
be sufficiently in advance of the oral presentation to allow interested 
persons to participate. If the oral presentation involves a proposed 
rule, the notice of opportunity may be in the notice proposing the rule 
or in a later, separate Federal Register notice.



Sec. 1052.3  Conduct of oral presentation.

    (a) The purpose of the oral presentation is to afford interested 
persons an opportunity to participate in person in the Commission's 
rulemaking or other proceedings and to help inform the Commission of 
relevant data, views and arguments.
    (b) The oral presentation, which shall be taped or transcribed, 
shall be an informal, non-adversarial legislative-type proceeding at 
which there will be no formal pleadings or adverse parties.
    (c) The proceedings for the oral presentation shall be conducted 
impartially, thoroughly, and expeditiously to allow interested persons 
an opportunity for oral presentation of data, views or arguments.



Sec. 1052.4  Presiding officer; appointment, duties, powers.

    (a) For oral presentations, the presiding officer shall either be 
the Chairman of the Commission or a presiding officer shall be appointed 
by the Chairman with the concurrence of the Commission.
    (b) The presiding officer shall chair the proceedings, shall make 
appropriate provision for testimony, comments and questions, and shall 
be responsible for the orderly conduct of the proceedings. The presiding 
officer shall have all the powers necessary or appropriate to contribute 
to the equitable and efficient conduct of the oral proceedings including 
the following:
    (1) The right to apportion the time of persons making presentations 
in an equitable manner in order to complete the presentations within the 
time period allotted for the proceedings.
    (2) The right to terminate or shorten the presentation of any party 
when, in the view of the presiding officer, such presentation is 
repetitive or is not relevant to the purpose of the proceedings.
    (3) The right to confine the presentations to the issues specified 
in the notice of oral proceeding or, where no issues are specified, to 
matters pertinent to the proposed rule or other proceeding.
    (4) The right to require a single representative to present the 
views of two or more persons or groups who have

[[Page 138]]

the same or similar interests. The presiding officer shall have the 
authority to identify groups or persons with the same or similar 
interests in the proceedings.
    (c) The presiding officer and Commission representatives shall have 
the right to question persons making an oral presentation as to their 
testimony and any other relevant matter.



PART 1061--APPLICATIONS FOR EXEMPTION FROM PREEMPTION--Table of Contents




Sec.
1061.1 Scope and purpose.
1061.2 Definitions.
1061.3 Statutory considerations.
1061.4 Threshold requirements for applications for exemption.
1061.5 Form of applications for exemption.
1061.6 Contents of applications for exemption.
1061.7 Documentation of the State or local requirement.
1061.8 Information on the heightened degree of protection afforded.
1061.9 Information about the effect on interstate commerce.
1061.10 Information on affected parties.
1061.11 Incomplete or insufficient applications.
1061.12 Commission consideration on merits.

    Authority: 15 U.S.C. 2075; 15 U.S.C. 1261n; 15 U.S.C. 1203; 15 
U.S.C. 1476.

    Source: 56 FR 3416, Jan. 30, 1991, unless otherwise noted.



Sec. 1061.1  Scope and purpose.

    (a) This part applies to the submission and consideration of 
applications by State and local governments for exemption from 
preemption by statutes, standards, and regulations of the Consumer 
Product Safety Commission.
    (b) This part implements section 26 of the Consumer Product Safety 
Act (CPSA) (15 U.S.C. 2075), section 18 of the Federal Hazardous 
Substances Act (FHSA) (15 U.S.C. 1261n), section 16 of the Flammable 
Fabrics Act (FFA) (15 U.S.C. 1203), and section 7 of the Poison 
Prevention Packaging Act (PPPA) (15 U.S.C. 1476), all as amended.



Sec. 1061.2  Definitions.

    For the purposes of this part:
    (a) Commission means the Consumer Product Safety Commission.
    (b) Commission's statutory preemption provisions and statutory 
preemption provisions means section 26 of the CPSA (15 U.S.C. 2075), 
section 18 of the FHSA (15 U.S.C. 1261n), section 16 of the FFA (15 
U.S.C. 1203) and section 7 of the PPPA (15 U.S.C. 1476).
    (c) Commission statute, standard, or regulation means a statute, 
standard, regulation, or requirement that is designated as having a 
preemptive effect by the Commission's statutory preemption provisions.
    (d) State means a State, the District of Columbia, the Commonwealth 
of Puerto Rico, the Virgin Islands, Guam, Wake Island, Midway Island, 
Kingman Reef, Johnston Island, the Canal Zone, American Samoa, or the 
Trust Territory of the Pacific Islands.
    (e) Local government means any political subdivision of a State 
having the authority to establish or continue in effect any standard, 
regulation, or requirement that has the force of law and is applicable 
to a consumer product.
    (f) State or local requirement means any statute, standard, 
regulation, ordinance, or other requirement that applies to a product 
regulated by the Commission, that is issued by a State or local 
government, and that is intended to have the force of law when in 
effect.



Sec. 1061.3  Statutory considerations.

    (a) The Commission's statutory preemption provisions provide, 
generally, that whenever consumer products are subject to certain 
Commission statutes, standards, or regulations, a State or local 
requirement applicable to the same product is preempted, i.e., 
superseded and made unenforceable, if both are designed to protect 
against the same risk of injury or illness, unless the State or local 
requirement is identical to the Commission's statutory requirement, 
standard, or regulation. A State or local requirement is not preempted 
if the product it is applicable to is for the State or local 
government's own use and the requirement provides a higher degree of 
protection than the Commission's statutory requirement, standard, or 
regulation.
    (b) The Commission's statutory preemption provisions provide, 
generally, that if a State or local government

[[Page 139]]

wants to enforce its own requirement that is preempted, the State or 
local government must seek an exemption from the Commission before any 
such enforcement. The Commission may, by regulation, exempt a State or 
local requirement from preemption if it finds that the State or local 
requirement affords a significantly higher degree of protection than the 
Commission's statute, standard, or regulation, and that it does not 
unduly burden interstate commerce. Such findings must be included in any 
exemption regulation.



Sec. 1061.4  Threshold requirements for applications for exemption.

    (a) The Commission will consider an application for preemption on 
its merits, only if the application demonstrates all of the following:
    (1) The State or local requirement has been enacted or issued in 
final form by an authorized official or instrumentality of the State or 
local government. For purposes of this section, a State or local 
requirement may be considered to have been enacted or issued in final 
form even though it is preempted by a Commission standard or regulation.
    (2) The applicant is an official or instrumentality of a State or 
local government having authority to act for, or on behalf of, that 
government in applying for an exemption from preemption for the safety 
requirement referred to in the application.
    (3) The State or local requirement is preempted under a Commission 
statutory preemption provision by a Commission statute, standard, or 
regulation. A State or local requirement is preempted if the following 
tests are met:
    (i) There is a Commission statute, standard, or regulation in effect 
that is applicable to the product covered by the State or local 
requirement.
    (ii) The Commission statute, standard, or regulation is designated 
as having a preemptive effect under a statutory preemption provision.
    (iii) The State or local requirement is designed to protect against 
the same risk of injury or illness as that addressed by the Commission 
statute, standard, or regulation.
    (iv) The State or local requirement is not identical to the 
Commission statute, standard, or regulation.
    (b) State and local governments may contact the Commission's Office 
of the General Counsel to obtain informal advice on whether a State or 
local requirement meets the threshold requirements of paragraph (a) of 
this section.



Sec. 1061.5  Form of applications for exemption.

    An application for exemption shall:
    (a) Be written in the English language.
    (b) Clearly indicate that it is an application for an exemption from 
preemption by a Commission statute, standard, or regulation.
    (c) Identify the State or local requirement that is the subject of 
the application and give the date it was enacted or issued in final 
form.
    (d) Identify the specific Commission statute, standard, or 
regulation that is believed to preempt the State or local requirement.
    (e) Contain the name and address of the person, branch, department, 
agency, or other instrumentality of the State or local government that 
should be notified of the Commission's actions concerning the 
application.
    (f) Document the applicant's authority to act for, or on behalf of, 
the State or local government in applying for an exemption from 
preemption for the particular safety requirement in question.
    (g) Be signed by an individual having authority to apply for the 
exemption from federal preemption on behalf of the applicant.
    (h) Be submitted, in five copies, to the Secretary, Consumer Product 
Safety Commission, Washington, DC 20207.



Sec. 1061.6  Contents of applications for exemption.

    Applications for exemption shall include the information specified 
in Sec. Sec. 1061.7 through 1061.10. More generally, a State or local 
government seeking an exemption should provide the Commission with the 
most complete information possible in support of the findings the 
Commission is required to make in issuing an exemption

[[Page 140]]

regulation. If any of the specified information is omitted because it is 
unavailable or not relevent, such omission should be explained in the 
application.



Sec. 1061.7  Documentation of the State or local requirement.

    An application for an exemption from preemption shall contain the 
following information:
    (a) A copy of the State or local requirement that is the subject of 
the application. Where available, the application shall also include 
copies of any legislative history or background materials used in 
issuing the requirement, including hearing reports or studies concerning 
the development or consideration of the requirement.
    (b) A written explanation of why compliance with the State or local 
requirement would not cause the product to be in violation of the 
applicable Commission statute, standard, or regulation.



Sec. 1061.8  Information on the heightened degree of protection afforded.

    An application for an exemption from preemption shall also contain 
information demonstrating that the State or local requirement provides a 
significantly higher degree of protection from the risk of injury or 
illness than the preempting Commission statute, standard, or regulation. 
More specifically, an application shall contain:
    (a) A description of the risk of injury or illness addressed by the 
State or local requirement.
    (b) A detailed explanation of the State or local requirement and its 
rationale.
    (c) An analysis of differences between the State or local 
requirement and the Commission statute, standard, or regulation.
    (d) A detailed explanation of the State or local test method and its 
rationale.
    (e) Information comparing available test results for the Commission 
statute, standard, or regulation and the State or local requirement.
    (f) Information to show hazard reduction as a result of the State or 
local requirement, including injury data and results of accident 
simulation.
    (g) Any other information that is relevant to applicant's contention 
that the State or local requirement provides a significantly higher 
degree of protection than does the Commission statute, standard, or 
regulation.
    (h) Information regarding enforcement of the State or local 
requirement and sanctions that could be imposed for noncompliance.



Sec. 1061.9  Information about the effect on interstate commerce.

    An application for exemption from preemption shall provide 
information on the effect on interstate commerce a granting of the 
requested exemption would be expected to cause, including the extent of 
the burden and the benefit to public health and safety that would be 
provided by the State or local requirement. More specifically, 
applications for exemption shall include, where available, information 
showing:
    (a) That it is technologically feasible to comply with the State or 
local requirement. Evidence of technological feasibility could take the 
form of:
    (1) Statements by affected persons indicating ability to comply with 
the State or local government requirement.
    (2) Statements indicating that other jurisdictions have established 
similar requirements that have been, or could be, met by persons 
affected by the requirement that is the subject of the application.
    (3) Information as to technological product or process modifications 
necessary to achieve compliance with the State or local requirement.
    (4) Any other information indicating the technological feasibility 
of compliance with the State or local requirement.
    (b) That it is economically feasible to comply with the State or 
local requirement, i.e., that there would not be significant adverse 
effects on the production and distribution of the regulated products. 
Evidence of economic feasibility could take the form of:
    (1) Information showing that the State or local requirement would 
not result in the unavailability (or result in a significant decline in 
the availability) of the product, either in the

[[Page 141]]

interstate market or within the geographic boundary of the State or 
local government imposing the requirement.
    (2) Statements from persons likely to be affected by the State or 
local requirement concerning the anticipated effect of the requirement 
on the availability or continued marketing of the product.
    (3) Any other information indicating the economic impact of 
compliance with the State or local requirement, such as projections of 
the anticipated effect of the State or local requirement on the sales 
and prices of the product, both in interstate commerce and within the 
geographic area of the State or local government.
    (c) The present geographic distribution of the product to which the 
State or local requirement would apply, and projections of future 
geographic distribution. Evidence of the geographic distribution could 
take the form of governmental or private information or data (including 
statements from manufacturers, distributors, or retailers of the 
product) showing advertising in the interstate market, interstate 
retailing, or interstate distribution.
    (d) The probability of other States or local governments applying 
for an exemption for a similar requirement. Evidence of the probability 
that other States or local governments would apply for an exemption 
could take the form of statements from other States or local governments 
indicating their intentions.
    (e) That specified local conditions require the State or local 
government to apply with the exemption in order to adequately protect 
the public health or safety of the State or local area.



Sec. 1061.10  Information on affected parties.

    An application for an exemption from preemption shall include a 
statement which identifies in general terms, parties potentially 
affected by the State or local requirement, especially small businesses, 
including manufacturers, distributors, retailers, consumers, and 
consumer groups.



Sec. 1061.11  Incomplete or insufficient applications.

    (a) If an application fails to meet the threshold requirements of 
Sec. 1061.4(a) of this part, the Office of General Counsel will inform 
the applicant and return the application without prejudice to its being 
resubmitted.
    (b) If an application fails to provide all the information specified 
in Sec. Sec. 1061.5 through 1061.10 of this part, and fails to fully 
explain why it has not been provided, the Office of General Counsel will 
either:
    (1) Return it to the applicant without prejudice to its being 
resubmitted,
    (2) Notify the applicant and allow it to provide the missing 
information, or
    (3) If the deficiencies are minor and the applicant concurs, forward 
it to the Commission for consideration on its merits.
    (c) If the Commission or the Commission staff believes that 
additional information is necessary or useful for a proper evaluation of 
the application, the Commission or Commission staff will promptly 
request the applicant to furnish such additional information.
    (d) If an application is not returned under paragraphs (a) or (b) of 
this section, the Commission will consider it on its merits.



Sec. 1061.12  Commission consideration on merits.

    (a) If the Commission proposes to grant an application for exemption 
it will, in accordance with 5 U.S.C. 553, publish a notice of that fact 
in the Federal Register, including a proposed exemption regulation, and 
provide an opportunity for written and oral comments on the proposed 
exemption by any interested party.
    (b) The Commission will evaluate all timely written and oral 
submissions received from interested parties, as well as any other 
available and relevant information on the proposal.
    (c) The Commission's evaluation will focus on:
    (1) Whether the State or local requirement provides a significantly 
higher degree of protection than the Commission statute or regulation 
from the risk of injury or illness that they both address.

[[Page 142]]

    (2) Whether the State or local requirement would unduly burden 
interstate commerce if the grant of the exemption from preemption allows 
it to go into effect. The Commission will evaluate these factors in 
accordance with the Commission's statutory preemption provisions and 
their legislative history.
    (3) Whether compliance with the State or local requirements would 
not cause the product to be in violation of the applicable Commission 
statute, standard, or regulation.
    (d) If, after evaluating the record, the Commission determines to 
grant an exemption, it will publish a final exemption regulation, 
including the findings required by the statutory preemption provisions, 
in the Federal Register.
    (e) If the Commission denies an application, whether or not 
published for comment, it will publish its reasons for doing so in the 
Federal Register.

[[Page 143]]