관리1 CGMP for Finished Pharmaceuticals –Subpart E Subpart E - Control of Components and Drug Product Containers and Closures Subpart E – 원료, 의약품 용기, 마개의 관리 Sec. 211.80 General requirements. Sec. 211.80 공통 (a) There shall be written procedures describing in sufficient detail the receipt, identification, storage, handling, sampling, testing, and approval or rejection of components and drug product containers and closures; such written procedures .. 2021. 8. 5. 이전 1 다음