[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]
 BILLING CODE 4164-01-P


