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 ● Halaman 327 ● ISBN 9781439829462 ● Editor Mel (University of Washington, Seattle, USA) Koch & Duncan (Amgen, Thousand Oaks, California, USA) Low ● Penerbit CRC Press ● Diterbitkan 2011 ● Diunduh 6 kali ● Mata uang EUR ● ID 2382013 ● Perlindungan salinan Adobe DRM
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