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2004.06.08

バリデーション報告書の目的

2004.06.01

ＩＱの目的

2001.01.13

ICH Q7 原薬GMPのガイドライン（平成13年11月 2 日、薬発第1200号）

1997.08.20

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Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

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