85 FR 133 pg. 41591 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 85Number: 133Page: 41591
Page: 41591Docket number: [Docket Nos. FDA-2018-N-2434, FDA-2016-N-3535, FDA-2013-N-1619, FDA-2016-N-0736, FDA-2019-N-3885, FDA-2013-N-1423, FDA-2013-N-0804, FDA-2016-N-3995, FDA-2018-D-1592, FDA-2016-N-2066, and FDA-2017-N-0366]
FR document: [FR Doc. 2020-14875 Filed 7-9-20; 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-2018-N-2434, FDA-2016-N-3535, FDA-2013-N-1619, FDA-2016-N-0736, FDA-2019-N-3885, FDA-2013-N-1423, FDA-2013-N-0804, FDA-2016-N-3995, FDA-2018-D-1592, FDA-2016-N-2066, and FDA-2017-N-0366]
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 |
|---|---|---|
| Formal Meetings Between the Food and Drug Administration and Sponsors and Applicants of Prescription Drug User Fee Act Products | 0910-0429 | 5/31/2023 |
| Special Protocol Assessments | 0910-0470 | 5/31/2023 |
| Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements | 0910-0606 | 5/31/2023 |
| Tracking Network for PETNet, LivestockNet, and SampleNet | 0910-0680 | 5/31/2023 |
| Center for Tobacco Products, Food and Drug Administration Funded Trainee/Scholar Survey | 0910-0887 | 5/31/2023 |
| Importer's Entry Notice | 0910-0046 | 6/30/2023 |
| Premarket Notification Submission 510(k), Subpart E | 0910-0120 | 6/30/2023 |
| Medical Devices; Pediatric Uses of Devices; Requirement for Submission of Information on Pediatric Subpopulations | 0910-0748 | 6/30/2023 |
| Controlled Correspondence Related to Generic Drug Development | 0910-0797 | 6/30/2023 |
| Certification of Identity for Freedom of Information Act and Privacy Act Requests | 0910-0832 | 6/30/2023 |
| FDA Advisory Committee Membership Nominations | 0910-0833 | 6/30/2023 |
Dated: July 6, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-14875 Filed 7-9-20; 8:45 am]
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