84 FR 177 pgs. 48151-48152 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 84Number: 177Pages: 48151 - 48152
Pages: 48151, 48152Docket number: [Docket Nos. FDA-2018-N-3516, FDA 2019-N-0482, FDA-2012-N-0021, FDA-2018-N-4042, FDA-2011-D-0597, FDA-2018-N-4735, FDA-2019-N-0721, FDA-2013-N-1425, FDA-2018-D-3631, and FDA-2011-D-0689]
FR document: [FR Doc. 2019-19779 Filed 9-11-19; 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-3516, FDA 2019-N-0482, FDA-2012-N-0021, FDA-2018-N-4042, FDA-2011-D-0597, FDA-2018-N-4735, FDA-2019-N-0721, FDA-2013-N-1425, FDA-2018-D-3631, and 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:
[top] The Food and Drug Administration (FDA) is publishing a
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.
| Title of collection | OMB control No. | Date approval expires |
|---|---|---|
| Disease Awareness and Prescription Drug Promotion on Television | 0910-0874 | 8/31/2021 |
| Reporting Associated with New Animal Drug Applications and Veterinary Master Files | 0910-0032 | 7/31/2022 |
| Substances Generally Recognized as Safe: Notification Procedure | 0910-0342 | 7/31/2022 |
| Establishing and Maintaining Lists of U.S. Product Manufacturers/Processors with Interest in Exporting CFSAN-Regulated Products | 0910-0509 | 7/31/2022 |
| Oversight of Clinical Investigations; A Risk-Based Approach to Monitoring | 0910-0733 | 7/31/2022 |
| Safety Labeling Changes; Implementation of the Federal Food, Drug, and Cosmetic Act | 0910-0734 | 7/31/2022 |
| Accreditation of Third Party Certification Bodies to Conduct Food Safety Audits and Issue Certifications | 0910-0750 | 7/31/2022 |
| Mitigation Strategies to Protect Food Against Intentional Adulteration | 0910-0812 | 7/31/2022 |
| Standards for the Growing, Harvesting, Packaging, and Holding of Produce for Human Consumption | 0910-0816 | 7/31/2022 |
| De Novo Classification Process (Evaluation of Automatic Class III Designation) | 0910-0844 | 8/31/2022 |
Dated: September 6, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-19779 Filed 9-11-19; 8:45 am]
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