미국지엪피1 CGMP for Finished Pharmaceuticals –Subpart A 21 CFR Part 211. Current Good Manufacturing Practice for Finished Pharmaceuticals. Subpart A - General Provisions Subpart A – 공통 Sec. 211.1 Scope. 211.1절 적용범위 (a) The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products (excluding positron emission tomography drugs) for administration to humans or animals. 사람 또는 동물 의약품(PET 의약품 제외) 제조를 .. 2021. 6. 15. 이전 1 다음