权威医学用药书籍速查系统

6. QUALIFICATION OF DEGRADATION PRODUCTS

Qualification is the process of acquiring and evaluating data that establishes the biological safety of an individual degradation product or a given degradation profile at the level ( s ) specified .Justification of such higher levels should include consideration of factors such as : the amount of degradation product administered in previous safety and/or clinical studies and found to be safe.

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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 > IMPURITIES?IN?NEW?DRUG?PRODUCTS Q3B(R2) > IMPURITIES IN NEW DRUG PRODUCTS
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:254-257
版本:1
出版时间:2011-01-01
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