Notices. Notice
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/register/2017/11/06/2017-24121A 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-2010-N-0258; FDA-2010-N-0623; FDA-2007-N-0383; FDA-2009-N-0360; FDA-2016-N-4620; FDA-2013-N-1496; FDA-2007-N-0220; FDA-2017-N-1848; FDA-2017-N-1066; FDA-2015-D-3327; FDA-2011-D-0689] 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 Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission to Information to a Master File in Support of Petitions; and Electronic Submission Using FDA 3053 0910-0016 9/30/2020 Voluntary Cosmetic Registration Program 0910-0027 9/30/2020 Radioactive Drug Research Committees 0910-0053 9/30/2020 FDA Safety Communication Readership Survey 0910-0341 9/30/2020 Medical Devices; Reports for Corrections and Removals 0910-0359 9/30/2020 Generic FDA Rapid Response Surveys 0910-0500 9/30/2020 Guidance for Industry: Pharmacogenomic Data Submissions 0910-0557 9/30/2020 Cosmetic Labeling Regulations 0910-0599 9/30/2020 Annual Reporting for Custom Device Exemption 0910-0767 9/30/2020 GFI: E6(R2) Good Clinical Practice; International Council for Harmonisation 0910-0843 9/30/2020 DeNovo Classification Process (Evaluation of Automatic Class II Designation) 0910-0844 9/30/2020 Dated: November 1, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. [FR Doc. 2017-24121 Filed 11-3-17; 8:45 am]
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