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Biotechnology and Bioprocessing

446,70 €

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 (QbD) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the rapid growth in the biopharmaceutical area and the comp

ISBN
9781439829462
Språk
engelska
Utgivningsdatum
7.12.2011
Förlag
CRC Press