As with all of pharmaceutical production, the regulatory environment for the production of therapeutics has been changing as a direct result of the US FDA-initiated Quality by Design (Qb D) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the rapid growth in the biopharmaceutical area and the comp
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Format PDF ● Pages 327 ● ISBN 9781439829462 ● Éditeur Mel (University of Washington, Seattle, USA) Koch & Duncan (Amgen, Thousand Oaks, California, USA) Low ● Maison d’édition CRC Press ● Publié 2011 ● Téléchargeable 6 fois ● Devise EUR ● ID 2382013 ● Protection contre la copie Adobe DRM
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