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# Biologic Adverse Event Info Collection
- URL: https://www.fdaweb.com/biologic-adverse-event-info-collection/
- Published: 2023-09-28T12:00:00.000Z
- Updated: 2026-09-14T18:59:06.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5155440

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “Adverse Experience Reporting For Licensed Biological Products; and General Records — 21 CFR Part 600.” The collection supports the agency’s regulatory authorities that govern adverse experience reporting after a biological product is approved and enters the market. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2023-09-28/pdf/2023-21252.pdf?ref=fdaweb.com).