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Biographie et livres de Christopher M. Riley

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Dr. Christopher Riley is the President of Riley and Rabel Consulting Services. He received a bachelor’s degree in Pharmacy (1977) and PhD degree in Pharmaceutical Chemistry (1980) from the University of Bath, UK. He taught Pharmaceutical Chemistry, at the Universities of Florida (1983-6) and the University of Kansas (1986-94), and was a Vice President at DuPont Merck (1994-2001) and ALZA (a division of J&J) (2001-7). He has coauthored more than 140 book chapters and papers in peer-reviewed journals, as well as 5 books. He has extensive experience in CMC regulatory affairs and the development of all types of dosage forms.
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Téléchargez le livre :  Specification of Drug Substances and Products
Specification of Drug Substances and Products

K. Lien Nguyen , Christopher M. Riley


Elsevier

2024-09-22

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Specification of Drug Substances and Drug Products is a fully comprehensive reference onSpecification Setting for Pharmaceuticals. There have been several recent developments in the ICH Guidelines, which were not captured in previous editions,...

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Télécharger le livre :  Specification of Drug Substances and Products
Specification of Drug Substances and Products: Development and Validation of Analytical Methods, Second Edition, presents a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis...

Editeur : Elsevier
Parution : 2020-07-23
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205,72

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Télécharger le livre :  Pharmaceutical and Biomedical Applications of Liquid Chromatography
This volume reflects the changes that have taken place in the pharmaceutical industry over the last ten years, most notably the increased importance attached to the question of chirality, the growing influence of biotechnology and the need for more rigorous...

Editeur : Pergamon
Parution : 2013-10-22
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Specification of Drug Substances and Products: Development and Validation of Analytical Methods is a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on phase-appropriate...

Editeur : Elsevier Science
Parution : 2013-08-21
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Télécharger le livre :  Development and Validation of Analytical Methods
The need to validate an analytical or bioanalytical method is encountered by analysts in the pharmaceutical industry on an almost daily basis, because adequately validated methods are a necessity for approvable regulatory filings. What constitutes a validated method,...

Editeur : Pergamon
Parution : 1996-05-29
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