83 FR 68 pgs. 15152-15153 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 83Number: 68Pages: 15152 - 15153
Pages: 15152, 15153Docket number: [Docket Nos. FDA-2014-N-0075; FDA-2011-N-0015; FDA-2011-N-0076; FDA-2017-N-0932; FDA-2016-N-4487; FDA-2014-N-0345; FDA-2013-N-0523; FDA-2017-N-2428; FDA-2008-N-0312; and FDA-2014-N-1072]
FR document: [FR Doc. 2018-07146 Filed 4-6-18; 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-2014-N-0075; FDA-2011-N-0015; FDA-2011-N-0076; FDA-2017-N-0932; FDA-2016-N-4487; FDA-2014-N-0345; FDA-2013-N-0523; FDA-2017-N-2428; FDA-2008-N-0312; and FDA-2014-N-1072]
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.
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| Title of collection | OMB Control No. | Date approval expires |
|---|---|---|
| Good Laboratory Practice Regulations for Nonclinical Studies | 0910-0119 | 1/31/2021 |
| Orphan Drug Designation Request Form and The Common European Medicines Agency/Food and Drug Administration Form for Orphan Medicinal Product Designation | 0910-0167 | 1/31/2021 |
| Electronic Records: Electronic Signatures | 0910-0303 | 1/31/2021 |
| Experimental Study on Warning Statements for Cigarette Graphic Health Warnings | 0910-0848 | 1/31/2021 |
| Consumer and Healthcare Professional Identification of and Responses to Deceptive Prescription Drug Promotion | 0910-0849 | 1/31/2021 |
| Data to Support Drug Product Communications | 0910-0695 | 2/28/2021 |
| Applications for FDA Approval to Market a New Drug | 0910-0001 | 3/31/2021 |
| Animal Drug Adverse Event Reporting and Recordkeeping | 0910-0284 | 3/31/2021 |
| Extralabel Drug Use in Animals | 0910-0325 | 3/31/2021 |
| Application for Participation in FDA Fellowship Programs | 0910-0780 | 3/31/2021 |
Dated: April 3, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-07146 Filed 4-6-18; 8:45 am]
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