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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Biçim PDF ● Sayfalar 327 ● ISBN 9781439829462 ● Editör Mel (University of Washington, Seattle, USA) Koch & Duncan (Amgen, Thousand Oaks, California, USA) Low ● Yayımcı CRC Press ● Yayınlanan 2011 ● İndirilebilir 6 kez ● Döviz EUR ● Kimlik 2382013 ● Kopya koruma Adobe DRM
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