[Federal Register Volume 76, Number 49 (Monday, March 14, 2011)]
[Notices]
[Pages 13620-13621]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-5732]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Opportunity to Partner; Testing of Patient Compartment Seating
and Restraints to Proposed Test Standard
Authority: 29 U.S.C. 669.
AGENCY: NIOSH, Centers for Disease Control and Prevention (CDC),
Department of Health and Human Services (HHS).
ACTION: Notice of informational meeting and opportunity to partner.
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SUMMARY: The National Institute for Occupational Safety and Health
(NIOSH), CDC, HHS, in collaboration with the National Truck Equipment
Association, Ambulance Manufacturers Division (NTEA-AMD) has developed
a series of proposed ambulance component test standards. One such
standard, AMD STANDARD 026--Seat, Seat Mount and Occupant Restraint
Dynamic Test--Proposed (draft), seeks to improve occupant and seat
retention during crash conditions. As a part of the standard
development process, NIOSH will be conducting a series of tests to
evaluate existing, redesigned, and/or new seating to validate the test
methods proposed. It is anticipated testing will be conducted in up to
three phases over approximately 15 months. NIOSH will contract with an
independent test facility and provide funding for all testing,
instrumentation, data collection, and data analysis. Prospective
industry partners will provide the following test assets: Seating, seat
retention devices, and occupant restraints. This project has three key
goals: (1) To validate test and data collection methodologies proposed
in AMD 026 (draft) to support standard development; (2) to support and
facilitate the transition of the industry from the current seating
design parameters to those proposed in SAE J2917 Surface Vehicle
Recommended Practice, Occupant Restraint and Equipment Mounting
Integrity--Frontal Impact System-Level Ambulance Patient Compartment,
published May 2010, and SAE J2956 Surface Vehicle Recommended Practice,
Occupant Restraint and Equipment Mounting Integrity--Side Impact
System-Level Ambulance Patient Compartment (draft); and, (3) to develop
the design and production ``cost-of-change'' to meet the proposed
design parameters.
Dates and Times: March 23, 2011, 1 p.m.-5 p.m., Eastern Standard Time
(EST) March 24, 2011, 8 a.m.-12 noon, EST, by appointment. NIOSH is
available to meet with individual companies for those interested in
further discussion. We anticipate offering the prospective partners the
opportunity to meet for 30 minutes, to ask specific questions pertinent
to their situation.
ADDRESSES: Homewood Suites Indianapolis-Downtown, 211 South Meridian
Street, Indianapolis, Indiana 46225, Telephone (317) 636-7992.
(Coincident with the 2011 Fire Department Instructors Conference
(FDIC).)
Letters of Interest: Interested manufacturers should submit a
letter of interest with information about their capabilities and level
of proposed participation to Jim Green at JGreen@cdc.gov. Letters of
interest must be received by April 25, 2011.
SUPPLEMENTARY INFORMATION: NIOSH proposes a series of up to 116 tests
to better understand the capabilities and limitations of currently
available seating and restraints, investigate redesign or new design
options, and validate the proposed test standard. As a byproduct of
this effort, it is expected that NIOSH and its partners will be able to
demonstrate that seating and restraints provided by partners meet the
design parameters specified in AMD 026 (draft) and test requirements
outlined in SAE J2917 and SAE 2956 (draft), respectively.
Prospective partners will be existing seating and/or restraint
manufacturers nationally or internationally. A prospective partner need
not be selling to the United States market at the time of this
announcement.
Prospective partners will be required to provide test assets
(seating, seat retention devices, and/or occupant restraints) free of
charge in exchange for their participation in this collaborative
standards development and validation effort. In return, NIOSH will
cover all costs associated with testing. This includes the cost of the
sled buck design and manufacture, rental of appropriate test manikins,
instrumentation related to the litter, manikin, and sled buck, test
execution, test data analysis, and cost data analysis.
Given the nature of the proposed change, coupled with the cost for
each unit, NIOSH anticipates the need to partner with more than one
manufacturer. Therefore no one manufacturer should expect to be asked
to contribute all needed test assets.
In phase 1, test assets are expected to come from those in the
existing product line per mutual agreement with NIOSH. In phases 2 and
3, test assets are expected to be introduced as either redesigns of
existing products or new products entirely based on the results of
phase 1 testing. The cost of product redesign and manufacture for phase
2 and 3 testing would be borne by the manufacturer partner(s).
Each partner will be invited to participate at the site of testing
(a third party independent test facility) during the testing of its
product. However, at no time will representatives from two different
manufacturers be present at the same time or on the same date. As a
participant, each partner will be provided with a copy of all digital
video and instrumented data for use in future product development.
NIOSH will retain a copy of all data but will code, to the extent
possible, to prevent release of vendor specific product data. Partners
will retain ownership of each test asset and will be asked to retrieve
test assets once each test has been completed. All shipping and/or
disposal costs of test assets to and from the independent test facility
will be borne by the manufacturer partner(s).
Recognizing any change in standard or test requirement may have a
coincident cost; NIOSH will also be seeking to quantify the cost of
change--that is, the cost of redesigning and manufacturing to meet the
proposed new test standards. In this instance, NIOSH has a separate
effort in place with an independent Certified Public Accountant (CPA).
Any participant or partner in this effort would be required to work
with the CPA in parallel with the test program outlined above.
Specifically, the partner would be required to provide the underlying
cost data for each product evaluated in the test program. This would
include the costs for a current or comparable pre-test or pre-standard
seat, seat retention device, and occupant restraint and its companion
post standard or post redesign equivalent. Prospective partners should
be aware it may be possible to consider a few products within their
existing product line (e.g.; entry level, mid level, and high end
products). These costs may include: Per
[[Page 13621]]
unit cost of materials, per unit cost of labor, per unit cost of
design, test and certification, etc. Data from each manufacturer will
be held confidential by the CPA and coded to remove corporate
identifiers. The goal is to assess the cost of change to the industry
rather than to an individual product within a given manufacturers'
broad product line.
Candidate companies will be evaluated based on their capability and
willingness to work cooperatively to achieve the stated goals.
Candidates selected will be required to enter into a Letter of
Agreement spelling out the level of participation expected of each
partner and the handling of data generated from the partnership. This
announcement does not obligate NIOSH to enter into an agreement with
any respondents. NIOSH reserves the right to establish a partnership
based on the engineering analysis and capabilities found by way of this
announcement or other searches, if determined to be in the best
interest of the government.
NIOSH recognizes this opportunity will raise many questions for
prospective partners. In order to give all involved the greatest
opportunity to understand the process and project expectations, the
NTEA-AMD, our collaborative partner and host standards setting body,
has agreed to provide a meeting room for us to hold an informational
meeting to present a broad overview of the effort and answer any
resulting questions.
In order to provide us with the best opportunity to meet the needs
of all prospective partners at each of these meetings; we request that
all interested parties contact Jim Green, NIOSH Project Officer, by e-
mail at JGreen@cdc.gov; or telephone (304) 285-5857, by Thursday, March
17, 2011.
CONTACT PERSON FOR MORE INFORMATION: Jim Green, NIOSH Project Officer,
e-mail: JGreen@cdc.gov; telephone (304) 285-5857.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of meetings and other committee management activities,
for both the Centers for Disease Control and Prevention and the Agency
for Toxic Substances and Disease Registry.
Dated: March 7, 2011.
Tanja Popovic,
Deputy Associate Director for Science, Centers for Disease Control and
Prevention.
[FR Doc. 2011-5732 Filed 3-11-11; 8:45 am]
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