Notices. Notice
309 words·~1 min read·
/register/2022/01/28/2022-01692A 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-0742; FDA-2018-N-0180; FDA-2019-N-2854; FDA-2021-N-0515; FDA-2014-N-1960; FDA-2017-D-6069; and FDA-2019-N-3325] 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 Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution 0910-0045 12/31/2024 Generic Clearance for the Collection of Qualitative Data on Tobacco Products and Communications 0910-0810 12/31/2024 Premarket Tobacco Product Applications and Recordkeeping Requirements 0910-0879 12/31/2024 Postmarketing Adverse Experience Reporting and Recordkeeping 0910-0230 1/31/2025 MedWatch: Adverse Event and Product Experience Reporting System (Paper Based) 0910-0291 1/31/2025 De Novo Classification Process (Evaluation of Automatic Class III Designation) 0910-0844 1/31/2025 Laboratory Accreditation for Analyses of Foods 0910-0898 1/31/2025 Dated: January 20, 2022. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2022-01692 Filed 1-27-22; 8:45 am]
Connectionstraces to 1
Traces to 1 document