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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
978-1-032-73011-0
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Advanced Aseptic Processing Technology
Taylor and Francis, 2024
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Freeze-Drying/Lyophilization of Pharmaceutical and Biological Products
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Generic Drug Product Development
Solid Oral Dosage Forms, Second Edition
Taylor and Francis, 2024
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Sterile Drug Products
Formulation, Packaging, Manufacturing and Quality
Taylor and Francis, 2024
978-1-032-91911-9
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livrable dans env. 10-20 jours
Industrial Hygiene in the Pharmaceutical and Consumer Healthcare Industries
Taylor and Francis, 2023
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livrable dans env. 10-20 jours
Good Manufacturing Practices for Pharmaceuticals, Seventh Edition
Taylor and Francis, 2021
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Biosimilar Drug Product Development
Taylor and Francis, 2020
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env. 126.00 CHF
livrable dans env. 10-20 jours
The Clinical Research Process in the Pharmaceutical Industry
Taylor and Francis, 2019
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env. 110.00 CHF
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Filtration and Purification in the Biopharmaceutical Industry, Third Edition
Taylor and Francis, 2019
978-1-138-05674-9
env. 416.00 CHF
livrable dans env. 10-20 jours
Pharmaceutical Powder Compaction Technology
Taylor and Francis, 2011
978-1-4200-8917-2
env. 300.00 CHF
livrable dans env. 10-20 jours
Pharmaceutical Process Scale-Up
Taylor and Francis, 2011
978-1-61631-001-1
env. 316.00 CHF
livrable dans env. 10-20 jours

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