Notices. Notice
403 words·~2 min read·
/register/2016/07/11/2016-16349A 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-2009-N-0221; FDA-2012-N-0559; FDA-2015-N-3287; FDA-2015-N-3815; FDA-2007-D-0429; FDA-2012-N-0447; FDA-2011-D-0597; FDA-2011-D-0164; FDA-2013-N-0013; FDA-2011-N-0146; FDA-2014-N-1533; FDA-2011-N-0921; FDA-2015-N-2163] 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 Food Labeling: Notification Procedures for Statements on Dietary Supplements 0910-0331 6/30/2019 PHS Guideline on Infectious Disease Issues in Xenotransplantation 0910-0456 6/30/2019 MDUFMA Small Business Qualification Certification 0910-0508 6/30/2019 Electronic Submission of Medical Device Registration and Listing 0910-0625 6/30/2019 Guidance for Industry on Q & A Regarding Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement & Nonprescription Drug Consumer Protection Act 0910-0641 6/30/2019 Antimicrobial Animal Drug Distribution Reports and Recordkeeping 0910-0659 6/30/2019 Guidance for Industry on Oversight of Clinical Investigations: A Risk-Based Approach to Monitoring 0910-0733 6/30/2019 Guidance for Industry on Safety Labeling Changes; Implementation of the Federal Food, Drug, and Cosmetic Act 0910-0734 6/30/2019 Accreditation of Third Party Certification Bodies to Conduct Food Safety Audits and Issue Certifications 0910-0750 6/30/2019 Sanitary Transportation of Human and Animal Food 0910-0773 6/30/2019 National Panel of Tobacco Consumer Studies 0910-0815 6/30/2019 Standards for the Growing, Harvesting, Packaging, and Holding of Produce for Human Consumption 0910-0816 6/30/2019 Hearing, Aging, and Direct-to-Consumer Television Advertisements 0910-0818 6/30/2019 Dated: July 6, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016-16349 Filed 7-8-16; 8:45 am]
Connectionstraces to 1
Traces to 1 document