Code of Federal Regulations · Part

Part 212 — Current Good Manufacturing Practice For Positron Emission Tomography Drugs

21 C.F.R. pt. 212

• 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 J Distribution
• Subpart K Complaint Handling
• Subpart L Records