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GMP Audits in Pharmaceutical and Biotechnology Industries
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GMP Audits in Pharmaceutical and Biotechnology Industries

Livre (relié)env. 226.00 CHF
livrable dans env. 10-20 jours

This user-friendly volume presents a basic knowledge on how to perform an audit or inspect a facility and meets all the needs of the audience. It is a key reference source for those training as auditors in organizations that follow FDA, EMA, MHRA, WHO, TGA, PIC/S regulations.

juin 2024, env. 546 pages, Drugs and the Pharmaceutical Sciences, Anglais
Taylor and Francis
978-1-03-225730-3

Autres titres de la collection: Drugs and the Pharmaceutical Sciences

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Pharmaceutical Process Engineering
Taylor and Francis, 2026
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Freeze-Drying/Lyophilization of Pharmaceutical and Biological Products
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Taylor and Francis, 2024
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Taylor and Francis, 2024
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Advanced Aseptic Processing Technology
Taylor and Francis, 2024
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Industrial Hygiene in the Pharmaceutical and Consumer Healthcare Industries
Taylor and Francis, 2023
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Good Manufacturing Practices for Pharmaceuticals, Seventh Edition
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Biosimilar Drug Product Development
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The Clinical Research Process in the Pharmaceutical Industry
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Filtration and Purification in the Biopharmaceutical Industry, Third Edition
Taylor and Francis, 2019
978-1-138-05674-9
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Pharmaceutical Powder Compaction Technology
Taylor and Francis, 2011
978-1-4200-8917-2
env. 300.00 CHF
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Pharmaceutical Process Scale-Up
Taylor and Francis, 2011
978-1-61631-001-1
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