GMP Audits in Pharmaceutical and Biotechnology Industries
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
Taylor and Francis
978-1-03-225730-3
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
Taylor and Francis
978-1-03-225730-3
Autres titres de la collection: Drugs and the Pharmaceutical Sciences
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Taylor and Francis, 2024
978-1-032-91845-7
85.00 CHF
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