Process Validation for Manufacturing of Terbinaforce Tablets的封面
书籍主题:

Process Validation for Manufacturing of Terbinaforce Tablets

Process Validation

LAP LAMBERT Academic Publishing (2020-05-05 )

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ISBN-13:

978-620-2-55341-4

ISBN-10:
6202553413
EAN:
9786202553414
书籍语言:
英文
作品简介:
SUMMARY- Validation is the way toward building up narrative proof exhibiting that a system, process, or movement did in testing and afterward creation keeps up the coveted level of consistence at all stages. In the pharmaceutical business, it is imperative that notwithstanding last testing and consistence of items, it is additionally guaranteed that the procedure will reliably deliver the normal outcomes. Validation mainly Based on, FDA regulations describing current good manufacturing practice (CGMP) for finished pharmaceuticals are provided in 21 CFR parts 210 and 211.A wide variety of procedures, processes, and activities need to be validated, the field of validation is divided into a number of subsections including the following:• Equipment validation• Facilities validation• HVAC system validation • Process Validation• Analytical method validation• Computer system validation• Packaging validation• Cold chain validation need of Process Validation for Assurance of quality of the product.
出版社 :
LAP LAMBERT Academic Publishing
网址:
https://www.lap-publishing.com/
由(作者):
Praveen Kumar, Meenu Chaudhary
页码 :
60
发表日期:
2020-05-05
现货:
备有现货
类别:
药学
价格:
39.90 €
关键词:
Process Validation, manufacturing of terbinaforce tablets

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