81 FR 154 pgs. 52878-52879 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Type: NOTICEVolume: 81Number: 154Pages: 52878 - 52879
Pages: 52878, 52879Docket number: [Docket Nos. FDA-2014-N-1721; FDA-2012-N-0248; FDA-2011-N-0449; FDA-2012-N-0748; FDA-2012-N-0961; FDA-2012-N-0921; FDA-2014-N-0189; FDA-2004-N-0258]
FR document: [FR Doc. 2016-19021 Filed 8-9-16; 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-1721; FDA-2012-N-0248; FDA-2011-N-0449; FDA-2012-N-0748; FDA-2012-N-0961; FDA-2012-N-0921; FDA-2014-N-0189; FDA-2004-N-0258]
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:
FDA PRA Staff, Office of Operations, Food and Drug Administration, Three White Flint North, 10A63, 11601 Landsdown St., North Bethesda, MD 20852, 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 |
|---|---|---|
| Investigational New Drug Regulations | 0910-0014 | 2/28/2019 |
| Guidance for Industry on Formal Dispute Resolutions; Appeals Above the Division Level | 0910-0430 | 2/28/2019 |
| SPF Labeling and Testing Requirements for OTC Sunscreen Products | 0910-0717 | 2/28/2019 |
| Generic Drug User Fee Cover Sheet-Form FDA 3794 | 0910-0727 | 2/28/2019 |
| Environmental Impact Considerations | 0910-0322 | 4/30/2019 |
| FDA Adverse Event Reports; Electronic Submissions | 0910-0645 | 5/31/2019 |
| Importer's Entry Notice | 0910-0046 | 6/30/2019 |
| Exports: Notification and Recordkeeping Requirements | 0910-0482 | 6/30/2019 |
| Focused Mitigation Strategies to Protect Food Against Intentional Adulteration | 0910-0812 | 6/30/2019 |
Dated: August 5, 2016.
Jeremy Sharp,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2016-19021 Filed 8-9-16; 8:45 am]
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