21 C.F.R. Part 211
Current Good Manufacturing Practice for Finished Pharmaceuticals
AGeneral ProvisionsBOrganization and PersonnelCBuildings and FacilitiesDEquipmentEControl of Components and Drug Product Containers and ClosuresFProduction and Process ControlsGPackaging and Labeling ControlHHolding and DistributionILaboratory ControlsJRecords and ReportsKReturned and Salvaged Drug Products