82 FR 213 pgs. 51424-51425 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 82Number: 213Pages: 51424 - 51425
Pages: 51424, 51425Docket number: [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]
FR document: [FR Doc. 2017-24121 Filed 11-3-17; 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-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.
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 to Information to a Master File in Support of Petitions; and Electronic Submission Using FDA 3053 | 0910-0016 | 9/30/2020 |
| Voluntary Cosmetic Registration Program | 0910-0027 | 9/30/2020 |
| Radioactive Drug Research Committees | 0910-0053 | 9/30/2020 |
| FDA Safety Communication Readership Survey | 0910-0341 | 9/30/2020 |
| Medical Devices; Reports for Corrections and Removals | 0910-0359 | 9/30/2020 |
| Generic FDA Rapid Response Surveys | 0910-0500 | 9/30/2020 |
| Guidance for Industry: Pharmacogenomic Data Submissions | 0910-0557 | 9/30/2020 |
| Cosmetic Labeling Regulations | 0910-0599 | 9/30/2020 |
| Annual Reporting for Custom Device Exemption | 0910-0767 | 9/30/2020 |
| GFI: E6(R2) Good Clinical Practice; International Council for Harmonisation | 0910-0843 | 9/30/2020 |
| DeNovo Classification Process (Evaluation of Automatic Class II Designation) | 0910-0844 | 9/30/2020 |
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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