行政資料

• 事務連絡「医薬品添加剤GMP自主基準について」 2016/08/24
• PIC/S, GOOD PRACTICES FOR DATA MANAGEMENT AND INTEGRITY IN REGULATED GMP/GDP ENVIRONMENTS 2016/08/10
• WHO, Guidance on good data and record management practices 2016/05/16
• FDA, Data Integrity and Compliance With CGMP Guidance for Industry 2016/04/14

ページ

• 先頭へ
• 前へ
• …
• 52
• 53
• 54
• 55
• 56