权威医学用药书籍速查系统

2 . 3 Manufacturing Process Development

P . 3.3 ( i . e . , intended for commercial production batches ) should be explained .Appropriateness of the equipment used for the intended products should be discussed .Process development studies should provide the basis for process improvement , process validation , continuous process verification * ( where applicable ) , and any process control requirements .Where appropriate , such studies should address microbiological as well as physical and chemical attributes .

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——《2011药品注册的国际技术要求.质量部分》
书名:《2011药品注册的国际技术要求.质量部分》
栏目:2011药品注册的国际技术要求.质量部分 > PHARMACEUTICAL DEVELOPMENT Q8(R2) > PART I: PHARMACEUTICAL DEVELOPMENT > 2. PHARMACEUTICAL DEVELOPMENT
作者:美国ICH指导委员会 周海钧
参编:王执,王知坚,匡荣,李洋,张洁
页码:372-376
版本:1
出版时间:2011-01-01
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