Code of Federal Regulations · Part

Part 211 — Current Good Manufacturing Practice For Finished Pharmaceuticals

21 C.F.R. pt. 211

• Subpart A General Provisions
• Subpart B Organization And Personnel
• Subpart C Buildings And Facilities
• Subpart D Equipment
• Subpart E Control Of Components And Drug Product Containers And Closures
• Subpart F Production And Process Controls
• Subpart G Packaging And Labeling Control
• Subpart H Holding And Distribution
• Subpart I Laboratory Controls
• Subpart J Records And Reports
• Subpart K Returned And Salvaged Drug Products