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| 번호 | 제목 | 첨부파일 | 등록일 | 조회 |
|---|---|---|---|---|
| 공지 | 의료제품 GMP 관련 식약처 민원인 안내서 (가이드라인 해설서) 목록 | 2017.09.06 | 47,452 | |
| 공지 | 식약처 및 지방식약청 주관 2017년 2분기 설명회 자료 모음 | 2017.06.29 | 9,398 | |
| 97 | 2024 Emerging Trends In Cleanroom Technologies | 2024.09.10 | 30 | |
| 96 | Cleanrooms: What is the difference between clean-up period and recove... | 2024.09.10 | 37 | |
| 95 | The most common challenges with a cleanroom | 2024.09.10 | 30 | |
| 94 | The Real Cost Of Poor Quality — And What You Should Do About It | 2024.09.10 | 19 | |
| 93 | Draft Q&A Guidance Offers Roadmap For Biosimilar Post-approval Change... | 2024.08.08 | 138 | |
| 92 | 10 points on how the FDA's CDER monitors the Quality of Medicinal Pro... | 2024.08.08 | 142 | |
| 91 | The difference between an ISO 17025 certified laboratory and an ISO 9... | 2024.08.08 | 156 | |
| 90 | This Week at FDA: Updated guidance on denying inspections and biosimi... | 2024.06.28 | 274 |
