[Federal Register Volume 82, Number 213 (Monday, November 6, 2017)]
[Notices]
[Pages 51424-51425]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-24121]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2010-N-0258; FDA-2010-N-0623; FDA-2007-N-0383; FDA-
2009-N-0360; FDA-2016-N-4620; FDA-2013-N-1496; FDA-2007-N-0220; FDA-
2017-N-1848; FDA-2017-N-1066; FDA-2015-D-3327; FDA-2011-D-0689]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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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: Ila S. Mizrachi, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-7726,
[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
https://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
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OMB control Date approval
Title of collection No. expires
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Submission of Petitions: Food Additive, 0910-0016 9/30/2020
Color Additive (Including Labeling),
Submission to Information to a Master
File in Support of Petitions; and
Electronic Submission Using FDA 3053...
Voluntary Cosmetic Registration Program. 0910-0027 9/30/2020
Radioactive Drug Research Committees.... 0910-0053 9/30/2020
FDA Safety Communication Readership 0910-0341 9/30/2020
Survey.................................
Medical Devices; Reports for Corrections 0910-0359 9/30/2020
and Removals...........................
Generic FDA Rapid Response Surveys...... 0910-0500 9/30/2020
Guidance for Industry: Pharmacogenomic 0910-0557 9/30/2020
Data Submissions.......................
Cosmetic Labeling Regulations........... 0910-0599 9/30/2020
Annual Reporting for Custom Device 0910-0767 9/30/2020
Exemption..............................
GFI: E6(R2) Good Clinical Practice; 0910-0843 9/30/2020
International Council for Harmonisation
DeNovo Classification Process 0910-0844 9/30/2020
(Evaluation of Automatic Class II
Designation)...........................
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Dated: November 1, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-24121 Filed 11-3-17; 8:45 am]
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