번호 | 제목 | 첨부파일 | 등록일 | 조회 |
---|---|---|---|---|
공지 | 의료제품 GMP 관련 식약처 민원인 안내서 (가이드라인 해설서) 목록 | 2017.09.06 | 47,252 | |
공지 | 식약처 및 지방식약청 주관 2017년 2분기 설명회 자료 모음 | 2017.06.29 | 9,246 | |
90 | This Week at FDA: Updated guidance on denying inspections and biosimi... | 2024.06.28 | 140 | |
89 | Are Annex 1's CCS Requirements Still Challenging You? | 2024.06.28 | 130 | |
88 | Requalification of an Automatic Inspection System (AVI) | 2024.06.28 | 115 | |
87 | EMA: Update of the Annex to the Excipients Guideline | 2024.06.28 | 63 | |
86 | New FDA Draft Guidance: Data Integrity For In Vivo Bioavailability An... | 2024.05.31 | 380 | |
85 | Euro Roundup: MHRA outlines potential impact of AI on medical product... | 2024.05.31 | 350 | |
84 | 4 things the first-ever RCC credential holders want you to know | 2024.05.31 | 356 | |
83 | Cleanrooms: Navigating regulators for environmental monitoring | 2024.05.31 | 263 |