Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is publishing a list of information collections that have Start Printed Page 24868been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (PRA).
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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.
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The following is a list of FDA information collections recently approved by OMB under section 3507 of the PRA (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|
|Applications for FDA Approval to Market a New Drug||0910-0001||3/31/2024|
|Medical Devices; Humanitarian Use Devices||0910-0332||3/31/2024|
|Medical Devices; Device Tracking||0910-0442||3/31/2024|
|Dispute Resolution Procedures for Science Based Decision on Products Regulated by CVM||0910-0566||3/31/2024|
|Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-Based In Vitro Diagnostics||0910-0850||3/31/2024|
|Assessment of Terms and Phrases Commonly Used in Prescription Drug Promotion||0910-0895||3/31/2024|
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Dated: May 4, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2021-09811 Filed 5-7-21; 8:45 am]
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