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
Dieses Ebook kaufen – und ein weitere GRATIS erhalten!
Format PDF ● Seiten 327 ● ISBN 9781439829462 ● Herausgeber Mel (University of Washington, Seattle, USA) Koch & Duncan (Amgen, Thousand Oaks, California, USA) Low ● Verlag CRC Press ● Erscheinungsjahr 2011 ● herunterladbar 6 mal ● Währung EUR ● ID 2382013 ● Kopierschutz Adobe DRM
erfordert DRM-fähige Lesetechnologie