Notices. Notice
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/register/2016/12/14/2016-30035·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-2013-N-0375; FDA-2013-N-0370; FDA-2013-N-0134; FDA-2009-N-0511; FDA-1997-N-0020; FDA-2011-N-0902; FDA-2013-N-0662; FDA-2013-N-0450; FDA-2012-N-0477; FDA-2013-N-0519] 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 Agreement for Shipments of Devices for Sterilization 0910-0131 9/30/2019 Export of Medical Devices—Foreign Letters of Approval 0910-0264 9/30/2019 Mammography Facilities, Standards, and Lay Summaries for Patients 0910-0309 9/30/2019 Medicated Fee Mill License Application 0910-0337 9/30/2019 Substances Generally Recognized as Safe: Notification Procedure 0910-0342 9/30/2019 Prescription Drug Product Labeling; Medication Guide Requirements 0910-0393 9/30/2019 Applications for FDA Approval to Market a New Drug: Patent Submission and Listing Requirements and Application of 30-month Stays on Approval of Abbreviated New Drug Applications Certifying That a Patent Claiming a Drug is Invalid or Will Not be Infringed 0910-0513 9/30/2016 Substances Prohibited from Use in Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed 0910-0339 10/31/2019 Investigational Device Exemptions Reports and Records—21 CFR 812 0910-0078 11/30/2019 Guidance for Industry on How to Submit Information in Electronic Format to the Center for Veterinary Medicine Using the FDA Electronic Submission Gateway 0910-0454 11/30/2019 Dated: December 9, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016-30035 Filed 12-13-16; 8:45 am]
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