[Federal Register Volume 81, Number 154 (Wednesday, August 10, 2016)]
[Notices]
[Pages 52878-52879]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-19021]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2014-N-1721; FDA-2012-N-0248; FDA-2011-N-0449; FDA-
2012-N-0748; FDA-2012-N-0961; FDA-2012-N-0921; FDA-2014-N-0189; FDA-
2004-N-0258]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is publishing a list of
information collections that have been approved by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A63, 11601
Landsdown St., North Bethesda, MD 20852, [email protected].
SUPPLEMENTARY INFORMATION: The following is a list of FDA information
collections recently approved by OMB under section 3507 of the
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control
number and expiration date of OMB approval for each information
collection are shown in table 1. Copies of the supporting statements
for the information collections are available on the Internet at http://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or
sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number.
Table 1--List of Information Collections Approved by OMB
------------------------------------------------------------------------
OMB control Date approval
Title of collection No. expires
------------------------------------------------------------------------
Investigational New Drug Regulations.... 0910-0014 2/28/2019
[[Page 52879]]
Guidance for Industry on Formal Dispute 0910-0430 2/28/2019
Resolutions; Appeals Above the Division
Level..................................
SPF Labeling and Testing Requirements 0910-0717 2/28/2019
for OTC Sunscreen Products.............
Generic Drug User Fee Cover Sheet--Form 0910-0727 2/28/2019
FDA 3794...............................
Environmental Impact Considerations..... 0910-0322 4/30/2019
FDA Adverse Event Reports; Electronic 0910-0645 5/31/2019
Submissions............................
Importer's Entry Notice................. 0910-0046 6/30/2019
Exports: Notification and Recordkeeping 0910-0482 6/30/2019
Requirements...........................
Focused Mitigation Strategies to Protect 0910-0812 6/30/2019
Food Against Intentional Adulteration..
------------------------------------------------------------------------
Dated: August 5, 2016.
Jeremy Sharp,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2016-19021 Filed 8-9-16; 8:45 am]
BILLING CODE 4164-01-P