84 FR 82 pgs. 18054-18055 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 84Number: 82Pages: 18054 - 18055
Pages: 18054, 18055Docket number: [Docket Nos. FDA-2018-N-2027; FDA-2012-N-0961; FDA-2018-N-3037; FDA-2014-N-1721; FDA-2005-N-0101; FDA-2012-N-0294; FDA-2011-N-0449; FDA-2018-N-3404; FDA-2018-N-3552; and FDA-2018-N-2969]
FR document: [FR Doc. 2019-08607 Filed 4-26-19; 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-2027; FDA-2012-N-0961; FDA-2018-N-3037; FDA-2014-N-1721; FDA-2005-N-0101; FDA-2012-N-0294; FDA-2011-N-0449; FDA-2018-N-3404; FDA-2018-N-3552; and FDA-2018-N-2969]
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.
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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 |
|---|---|---|
| Survey of Current Manufacturing Practices for the Cosmetic Industry | 0910-0867 | 3/31/2020 |
| Environmental Impact Considerations | 0910-0322 | 2/28/2022 |
| Generic Clearance for Quantitative Testing of the Development of Food and Drug Administration | 0910-0865 | 2/28/2022 |
| Investigational New Drug Regulations | 0910-0014 | 3/31/2022 |
| Prescription Drug User Fee Program | 0910-0297 | 3/31/2022 |
| Food Additives, Food Contact Substance Notification System | 0910-0495 | 3/31/2022 |
| SPF Labeling and Testing Requirements for OTC Sunscreen Products | 0910-0717 | 3/31/2022 |
| Generic Drug User Fee Program | 0910-0727 | 3/31/2022 |
| Experimental Study of Cigarette Warnings | 0910-0866 | 3/31/2022 |
| Assessment of Combination Product Review Practices | 0910-0868 | 3/31/2022 |
Dated: April 24, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-08607 Filed 4-26-19; 8:45 am]
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