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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 600 — BIOLOGICAL PRODUCTS: GENERAL
Subpart D — Reporting of Adverse Experiences
Federal (United States) · Regulations
Subpart D — Reporting of Adverse Experiences
4 sections
4 sections
21 C.F.R. § 600.80
Postmarketing reporting of adverse experiences.
21 C.F.R. § 600.81
Distribution reports.
21 C.F.R. § 600.82
Notification of a permanent discontinuance or an interruption in manufacturing.
21 C.F.R. § 600.90
Waivers.
Subpart D — Reporting of Adverse Experiences | Federal (United States) Regulations | Justis AI