Notices. Notice
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/register/2018/02/15/2018-03128·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA-2011-N-0424; FDA-2014-N-0192; FDA-2008-N-0094; FDA-2010-N-0062; FDA-2010-N-0588; FDA-2010-N-0110; FDA-2010-N-0493; FDA-2017-N-1095; FDA-2013-D-0349; FDA-2016-N-2683] 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. Table 1—List of Information Collections Approved by OMB Title of collection OMB control No. Date approval expires Temporary Marketing Permit Applications 0910-0133 11/30/2020 Establishing and Maintaining Lists of U.S. Milk Product Manufacturers/Processors with Interest in Exporting 0910-0509 11/30/2020 Channels of Trade Policy for Commodities with Residues of Pesticide Chemicals for Which Tolerances Have been Revoked, Suspended, or Modified by the EPA 0910-0562 11/30/2020 Medical Devices; Exception from General Requirements for Informed Consent 0910-0586 11/30/2020 Exceptions or Alternatives to Labeling Requirements for Products Held by the Strategic National Stockpile 0910-0614 11/30/2020 Prescription Drug Advertisements 0910-0686 11/30/2020 Additional Criteria and Procedures for Classifying Over-the-Counter Drugs as Generally Recognized as Safe and Effective and Not Misbranded 0910-0688 11/30/2020 Electronic Submission of Allegations of Regulatory Misconduct Associated with Medical Devices 0910-0769 11/30/2020 Providing Waiver-Related Materials in Accordance With the Guidance for Industry on Providing Post-Market Periodic Safety Reports in the International Conference on Harmonisation E2C(R2) Format 0910-0771 11/30/2020 Data To Support Social and Behavioral Research as Used by the Food and Drug Administration 0910-0847 11/30/2020 Dated: February 9, 2018. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2018-03128 Filed 2-14-18; 8:45 am]
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