85 FR 219 pg. 71925 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 85Number: 219Page: 71925
Page: 71925Docket number: [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]
FR document: [FR Doc. 2020-25022 Filed 11-10-20; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version: PDF Version
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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.
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.
| Title of collection | OMB control No. | Date approval expires |
|---|---|---|
| Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission of Information to a Master File in Support of Petitions, and Electronic Submission Using FDA Form 3503 | 0910-0016 | 09/30/2023 |
| 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 Exporting Covered Products to China | 0910-0884 | 09/30/2023 |
Dated: November 5, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-25022 Filed 11-10-20; 8:45 am]
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