Regulations.gov document

Electronic Submission of Expedited Safety Reports From Investigational New Drug-Exempt…

Notice · FDA-2022-D-1173 · posted Apr 2, 2024

Key facts

Document ID FDA-2022-D-1173-0003
Title Electronic Submission of Expedited Safety Reports From Investigational New Drug-Exempt Bioavailability/ Bioequivalence Studies; Guidance for Industry; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2022-D-1173
Posted Apr 2, 2024
Federal Register citation 89 FR 22728
FR document number 2024-06726
Comment period opens Apr 2, 2024
Effective date Apr 2, 2024

At a glance

  • 1–9 Pages
  • None Public comments on this docket

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