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

Buch (gebunden)ca. 226.00 CHF
lieferbar in ca. 10-20 Arbeitstagen

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.

Juni 2024, ca. 546 Seiten, Drugs and the Pharmaceutical Sciences, Englisch
Taylor and Francis
978-1-03-225730-3

Weitere Titel der Reihe: Drugs and the Pharmaceutical Sciences

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Pharmaceutical Process Engineering
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Solid Oral Dosage Forms, Second Edition
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Formulation, Packaging, Manufacturing and Quality
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Advanced Aseptic Processing Technology
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Industrial Hygiene in the Pharmaceutical and Consumer Healthcare Industries
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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
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