Part 212 — Current Good Manufacturing Practice for Positron Emission Tomography Drugs
Subpart A — General Provisions
Subpart B — Personnel and Resources
Subpart C — Quality Assurance
Subpart D — Facilities and Equipment
Subpart E — Control of Components, Containers, and Closures
Subpart F — Production and Process Controls
Subpart G — Laboratory Controls
Subpart H — Finished Drug Product Controls and Acceptance
Subpart I — Packaging and Labeling
Subpart K — Complaint Handling