Basics of Regulatory Affairs for Pharma Professional
Uitgelicht
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21,00 |
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33,20 |
Naar shop
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33,20 |
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Beschrijving
Bol
Pharma regulatory affairs, very difficult to understand for the person who wants to enter in the field of pharma and chemical industries. Here i have presented extract of different guideline in digestive language with all the difficult terminologies. Students of bachelors, masters, research scholars can easily select their career path in field of pharma regulatory affairs. The book contains basic idea of Quality, GMP, GLP, Validation, Impurity, Drug master file, calibration, Standard operating procedure, ICH guideline and Validation methodology. The book will surely fulfill the basic requirement of pharma regulatory affairs.
Beschrijving
(1)
Pharma regulatory affairs, very difficult to understand for the person who wants to enter in the field of pharma and chemical industries. Here i have presented extract of different guideline in digestive language with all the difficult terminologies. Students of bachelors, masters, research scholars can easily select their career path in field of pharma regulatory affairs. The book contains basic idea of Quality, GMP, GLP, Validation, Impurity, Drug master file, calibration, Standard operating procedure, ICH guideline and Validation methodology. The book will surely fulfill the basic requirement of pharma regulatory affairs.
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