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# Biologic Adverse Event Reporting Info Collection
- URL: https://www.fdaweb.com/biologic-adverse-event-reporting-info-collection/
- Published: 2024-03-12T12:00:00.000Z
- Updated: 2026-09-14T14:25:03.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5156536

*Federal Register* notice: FDA has submitted to OMB an information collection extension entitled “FDA Adverse Experience Reporting for Licensed Biological Products; and General Records — 21 CFR Part 600.” The collection supports statutory and regulatory authorities that govern adverse experience reporting. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2024-03-12/pdf/2024-05222.pdf?ref=fdaweb.com).