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1
Analytical chemistry an introduction to pharmaceutical GMP laboratory / Kim Huynh-Ba (editor)
Hoboken, NJ : John Wiley & Sons, Inc., 2022
xxx, 386 pages. : illustrations ; 24 cm.
Ký hiệu phân loại (DDC): 615.19
Analytical Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while maintaining compliance with Good Manufacturing Practices (GMP) regulations.
Số bản sách: (1) Tài liệu số: (1)
2
Handbook of stability testing in pharmaceutical development : regulations, methodologies, and best practices / [Editor] Kim Huynh-Ba
New York : Springer, 2009
389 p. : illustrations
Ký hiệu phân loại (DDC): 615
A comprehensive guide to stability testing in pharmaceutical development. It covers various aspects of stability testing in pharmaceutical development. It presents a scientific understanding of regulations and balances methodologies and best practices. It provides resources for pharmaceutical companies and educational institutions.
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