85 FR 179 pgs. 57220-57221 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 85Number: 179Pages: 57220 - 57221
Pages: 57220, 57221Docket number: [Docket Nos. FDA–2013–N–0618, FDA–2010–N–0601, FDA–2010–N–0598, FDA–2013–N–1155, FDA–2010–N–0118, FDA–2020–N–0145, FDA–2010–N–0597, FDA–2014–N–0086, FDA–2016–N–2836, FDA–2019–N–5841, and FDA–2019–N–5973]
FR document: [FR Doc. 2020–20332 Filed 9–14–20; 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-2013-N-0618, FDA-2010-N-0601, FDA-2010-N-0598, FDA-2013-N-1155, FDA-2010-N-0118, FDA-2020-N-0145, FDA-2010-N-0597, FDA-2014-N-0086, FDA-2016-N-2836, FDA-2019-N-5841, and FDA-2019-N-5973]
Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
AGENCY:
Food and Drug Administration, Health and Human Services (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 http://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.
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| Title of collection | OMB control No. | Date approval expires |
|---|---|---|
| Reporting and Recordkeeping for Electronic Products-General Requirements | 0910-0025 | 8/31/2023 |
| Current Good Manufacturing Practice Regulations for Medicated Feed | 0910-0152 | 8/31/2023 |
| Good Manufacturing Practice Regulations for Type A Medicated Articles, 21 CFR Part 226 | 0910-0154 | 8/31/2023 |
| Food Labeling Regulations | 0910-0381 | 8/31/2023 |
| Prior Notice of Imported Food Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002 | 0910-0520 | 8/31/2020 |
| Animal Drug User Fee Program | 0910-0540 | 8/31/2023 |
| Index of Legally Marketed Unapproved New Animal Drugs for Minor Species | 0910-0620 | 8/31/2023 |
| Potential Tobacco Product Violations Reporting Form | 0910-0716 | 8/31/2023 |
| Donor Risk Assessment Questionnaire for the FDA/National Heart, Lung, and Blood Institute-Sponsored Transfusion-Transmissible Infections Monitoring System-Risk Factor Elicitation | 0910-0841 | 8/31/2023 |
| Generic Clearance for Qualitative Data to Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed | 0910-0891 | 8/31/2023 |
| Health Care Providers Understanding of Opioid Analgesic Abuse-Deterrent Formulations: Phase 2 and 3 Surveys | 0910-0892 | 8/31/2023 |
Dated: September 9, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-20332 Filed 9-14-20; 8:45 am]
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