[Federal Register Volume 85, Number 219 (Thursday, November 12, 2020)]
[Notices]
[Page 71925]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-25022]



[[Page 71925]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2020-N-0908; FDA-2010-N-0583; FDA-2020-N-0257; FDA-
2008-N-0490; FDA-2011-N-0017; FDA-2011-N-0144; FDA-2015-D-3327; FDA-
2020-N-1207]


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, 
PRAStaff@fda.hhs.gov.

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, Color Additive (Including Labeling),          0910-0016       09/30/2023
 Submission of Information to a Master File in Support of Petitions, and
 Electronic Submission Using FDA Form 3503.....................................
Radioactive Drug Research Committees...........................................       0910-0053       09/30/2023
Rapid Response Surveys.........................................................       0910-0500       09/30/2023
Cosmetic Labeling and Voluntary Cosmetic Registration..........................       0910-0599       09/30/2023
Voluntary National Retail Food Regulatory Program Standards....................       0910-0621       09/30/2023
FDA's Voluntary Qualified Importer Program; Guidance for Industry..............       0910-0840       09/30/2023
GFI: E6(R2) Good Clinical Practice; International Council for Harmonisation....       0910-0843       09/30/2023
List of US Manufacturers of Specific CVM-Regulated Products with Interest in          0910-0884       09/30/2023
 Exporting Covered Products to China...........................................
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    Dated: November 5, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-25022 Filed 11-10-20; 8:45 am]
BILLING CODE 4164-01-P


