Author:
Edition: Softcover reprint of hardcover 1st ed. 2009
Binding: Paperback
ISBN: 1441927565
Edition: Softcover reprint of hardcover 1st ed. 2009
Binding: Paperback
ISBN: 1441927565
Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices
This handbook is the first to cover all aspects of stability testing in pharmaceutical development. It presents a scientific understanding of regulations and balances methodologies and best practices. Comprising 17 chapters, it provides a wealth of resources for pharmaceutical companies, educational institutions, and manufacturing laboratories to use as either a supplementary text for stability training courses or as a reference book for pharmaceutical practitioners. Topics covered include: (1) Latest regulations for stability testing, including cGMP requirements, ICH guidelines, and global guidances from WHO, ASEAN, EMRO, and other regions. (2) Post-approval considerations and regulatory filing strategies to support a global supply chain. (3) format hardback language english publication year 25 11 2008 subject medicine subject 2 clinical medicine professional title handbook of stability testing in pharmaceutical development regulations methodologies and best practices author huynh ba editor publisher springer verlag publication date dec 16 2008 pages 328 binding hardcover edition 1 st dimensions 6 14 wx 9 21 hx 0 94 d isbn 0387856269 subject medical pharmacology brand new hardcover all orders get full access to our online status tr Read medical textbooks online like Handbook of Stability Testing in Pharmaceutical Development here
Handbook Of Stability Testing In Pharmaceutical Development
Handbook Of Stability Testing In Pharmaceutical Development: Kim Huynh-Ba
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Store Search search Title, ISBN and Author Handbook of Stability Testing in Pharmaceutical Development Estimated delivery 3-12 business days Format Paperback Condition Brand New This handbook is the first to cover all aspects of stability testing in pharmaceutical development. Written by a group of international experts, the book presents a scientific understanding of regulations and balances methodologies and best practices. Publisher Description This handbook is the first to cover all aspects
Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices Springer 9781441927569 09781441927569
Handbook of Stability Testing in Pharmaceutical Development Online
It presents a scientific understanding of regulations and balances methodologies and best practices. Comprising 17 chapters, it provides a wealth of resources for pharmaceutical companies, educational institutions, and manufacturing laboratories to use as either a supplementary text for stability training courses or as a reference book for pharmaceutical practitioners. Topics covered include: (1) Latest regulations for stability testing, including cGMP requirements, ICH guidelines, and global guidances from WHO, ASEAN, EMRO, and other regions. (2) Post-approval considerations and regulatory filing strategies to support a global supply chain
t presents a scientific understanding of regulations and balances methodologies and best practices. Comprising 17 chapters, it provides a wealth of resources for pharmaceutical companies, educational institutions, and manufacturing laboratories to use as either a supplementary text for stability training courses or as a reference book for pharmaceutical practitioners. Topics covered include: (1) Latest regulations for stability testing, including cGMP requirements, ICH guidelines, and global guidances from WHO, ASEAN, EMRO, and other regions. (2) Post-approval considerations and regulatory filing strategies to support a global supply chain. (3)
