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Titlebook: Handbook of Stability Testing in Pharmaceutical Development; Regulations, Methodo Kim Huynh-Ba Book 2009 Springer-Verlag New York 2009 Deve

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書(shū)目名稱(chēng)Handbook of Stability Testing in Pharmaceutical Development
副標(biāo)題Regulations, Methodo
編輯Kim Huynh-Ba
視頻videohttp://file.papertrans.cn/423/422229/422229.mp4
概述This practical handbook is needed in this area to serve pharmaceutical scientists who handle responsibilities in a variety of functions relating to the drug stability, including R&D, formulation, anal
圖書(shū)封面Titlebook: Handbook of Stability Testing in Pharmaceutical Development; Regulations, Methodo Kim Huynh-Ba Book 2009 Springer-Verlag New York 2009 Deve
描述.A COMPREHENSIVE AND PRACTICAL GUIDE TO STABILITY TESTING IN PHARMACEUTICAL DEVELOPMENT...Stability testing is required to demonstrate that a pharmaceutical product meets its acceptance criteria throughout its shelf life and to gain regulatory approval for commercialization. Assessing drug product stability and safety can be quite complicated, and stability profile can impact many functional areas, including analytical testing, formulation development, toxicology, quality, and regulatory affairs....Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices is the first volume 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:....Latest regulations for stability testing, including cGMP requirements, ICH guidelines, and gl
出版日期Book 2009
關(guān)鍵詞Development; Huynh-Ba; Huynhba; Methodologies; Pharmaceutical; Regulations; Stability; Testing; drug
版次1
doihttps://doi.org/10.1007/978-0-387-85627-8
isbn_softcover978-1-4419-2756-9
isbn_ebook978-0-387-85627-8
copyrightSpringer-Verlag New York 2009
The information of publication is updating

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Kim Huynh-BaThis practical handbook is needed in this area to serve pharmaceutical scientists who handle responsibilities in a variety of functions relating to the drug stability, including R&D, formulation, anal
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Alvin J. Melveger,Kim Huynh-Baunity to rethink nuclear weapons policies and take significant steps towards a world free of nuclear weapons began to take shape. The re-emergence of an international nuclear disarmament agenda has placed the United Kingdom’s Trident replacement programme in a new international political context explored in this chapter.
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