89 FR 27 pg. 8682 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 89Number: 27Page: 8682
Page: 8682Docket number: [Docket Nos. FDA–2023–N–2894; FDA–2023–N–1929; FDA–2017–N–5569; FDA–2023–N–2564; FDA–2023–N–2851; FDA–2023–N–1554]
FR document: [FR Doc. 2024–02579 Filed 2–7–24; 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-2023-N-2894; FDA-2023-N-1929; FDA-2017-N-5569; FDA-2023-N-2564; FDA-2023-N-2851; FDA-2023-N-1554]
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:
Amber Sanford, Office of Operations, Food and Drug Administration, Three White Flint North, 10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-8867, 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 |
---|---|---|
Good Laboratory Practice (GLP) Regulations for Nonclinical Laboratory Studies | 0910-0119 | 1/31/2027 |
Orphan Drugs | 0910-0167 | 1/31/2027 |
Medical Devices; Device Tracking | 0910-0442 | 1/31/2027 |
Channels of Trade Policy for Commodities with Residues of Pesticide Chemicals for Which Tolerances Have Been Revoked, Suspended, or Modified by the EPA | 0910-0562 | 1/31/2027 |
Time and Extent Applications for Nonprescription Drug Products | 0910-0688 | 1/31/2027 |
Qualitative Feedback on Food and Drug Administration Service Delivery | 0910-0697 | 1/31/2027 |
Dated: February 5, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024-02579 Filed 2-7-24; 8:45 am]
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