HARMONIZATION IMPLEMENTATION OF CURRENT USP REQUIREMENT AND GAMP ON INSTRUMENT QUALIFICATION IN RESEARCH AND DEVELOPMENT LABORATORY WITH RISK MANAGEMENT APPROACH

Based on the requirement of the latest United State Pharmacopeia (USP), chapter 21 Code of Federal Regulation (CFR) part 11, and International Society for Pharmaceutical Engineering Good Automated Manufacturing Practice (ISPE GAMP), qualification of analytical instrument is the most basic things...

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主要作者: Kusuma Dewi Yatisantoso, Tias
格式: Theses
語言:Indonesia
在線閱讀:https://digilib.itb.ac.id/gdl/view/39904
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