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Guidelines for analytical method development and validation of biotechnological synthesis of drugs. Production of a chiral steroid as model
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Surface Biotechnology. Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical and Analytical Chemistry.
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Surface Biotechnology. Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical and Analytical Chemistry.
2003 (English)In: Journal of Chromatography B, Vol. 791, 323-336 p.Article in journal (Refereed) Published
Abstract [en]

In connection with biotechnological synthesis of pharmaceutical drugs, validated methods for quantification of both product and substrate at different time intervals are essential for proper calculation of rate coefficients. In this field, there still exi

Place, publisher, year, edition, pages
2003. Vol. 791, 323-336 p.
Keyword [en]
hydroxyprogesterones; validation
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URN: urn:nbn:se:uu:diva-48685OAI: oai:DiVA.org:uu-48685DiVA: diva2:76591
Available from: 2007-02-13 Created: 2007-02-13 Last updated: 2011-01-13

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