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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 212 — CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
Subpart H — Finished Drug Product Controls and Acceptance
Federal (United States) · Regulations
Subpart H — Finished Drug Product Controls and Acceptance
1 section
1 section
21 C.F.R. § 212.70
What controls and acceptance criteria must I have for my finished PET drug products?
Subpart H — Finished Drug Product Controls and Acceptance | Federal (United States) Regulations | Justis AI