ANURAG SINGH RATHORE, RATHORE (2021) PROCESS VALIDATION IN MANUFACTURING OF BIOPHARMACEUTICALS Guidelines, Current Practices, and Industrial Case Studies. T&F INFORMA PRESS.
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Pharmaceutical Master Validation Plan The Ultimate Guide to FDA, GMP, and GLP Compliance.pdf Download (2MB) |
Item Type: | Book |
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Subjects: | R Medicine > RZ Other systems of medicine |
Divisions: | Fakultas Farmasi > S1 Farmasi |
Depositing User: | tripayuni ekaputri |
Date Deposited: | 08 Jun 2021 03:39 |
Last Modified: | 08 Jun 2021 03:39 |
URI: | http://repo.upertis.ac.id/id/eprint/1837 |
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