How to Validate a Pharmaceutical Process
How to Validate a Pharmaceutical Process provides a "how to" approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behi...
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Main Author: | |
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Format: | Book |
Language: | English |
Published: |
AMSTERDAM
ELSEVIER
2016
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Series: | Expertise in pharmaceutical process technology series
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Subjects: | |
Online Access: | Click Here to View Status and Holdings. |
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020 | # | # | |a 9780128041482 |q paperback |
020 | # | # | |a 012804148X |q paperback |
040 | # | # | |a DNLM |d UiTM |e rda |
041 | 0 | # | |a eng |
060 | 0 | 0 | |a QV 771 |
090 | 0 | 0 | |a QV771 |b O857h 2016 |
100 | 1 | # | |a Ostrove, Steven A. |e author |
245 | 1 | 0 | |a How to Validate a Pharmaceutical Process |c Steven A. Ostrove |
264 | # | 1 | |a AMSTERDAM |b ELSEVIER |c 2016 |
264 | # | 4 | |c ©2016 |
300 | # | # | |a xviii, 199 pages |b illustrations, portrait |c 23 cm |
336 | # | # | |a text |2 rdacontent |
337 | # | # | |a unmediated |2 rdamedia |
338 | # | # | |a volume |2 rdacarrier |
490 | 1 | # | |a EXPERTISE IN PHARMACEUTICAL PROCESS TECHNOLOGY SERIES |
504 | # | # | |a Includes bibliographical references and index |
520 | # | # | |a How to Validate a Pharmaceutical Process provides a "how to" approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a pharmaceutical process. Understanding the "why" is critical to a successful and defensible process validation, making this book an essential research companion for all practitioners engaged in pharmaceutical process validation. |
546 | # | # | |a Text in English |
650 | # | 2 | |a Drug Industry |x standards |
650 | # | 2 | |a Quality Control |
650 | # | 2 | |a Legislation, Drug |
830 | # | 0 | |a Expertise in pharmaceutical process technology series |
856 | 4 | 0 | |z Click Here to View Status and Holdings. |u https://opac.uitm.edu.my/opac/detailsPage/detailsHome.jsp?tid=912274 |
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