Notices. Notice
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/register/2016/08/10/2016-19021·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4120-01-P 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. Table 1—List of Information Collections Approved by OMB 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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