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Biotechnology and Bioprocessing

4 459 kr
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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
2011-12-07
Förlag
CRC Press

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