株式会社極東書店トップ商品一覧Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices. 2009 ed.

商品詳細

Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices. 2009 ed.

Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices. 2009 ed.

・ISBN 978-0-387-85626-1 hard EUR 219.99

¥58,802.- (税込) (※)価格はご注文時の参考価格となります。
納品価格につきましては書籍の入荷時点で確定となります。
版元の原価改定、外国為替の変動等により異なる場合がございますので、予めご了承下さい。

お気に入り
著者・編者Huynh-Ba, Kim (ed.),
出版社 (Springer-Verlag New York Inc., US)
出版年月2008
ページ数389 pp.
言語ENG
ニュース番号<A05-34340>

解説

In my professional career as a pharmaceutical scientist, I have been involved with severalaspectsofthe drugdevelopmentprocessfrompre-INDto commercialization and, somehow, I usually found myself coming back to a stability-related issue. The stability area seemed to draw my utmost interest because in my day-to-day work, my opportunities involved more than one product, and none of the issues were the same.Eachsituationposedchallengesthatusuallyrequiredanexerciseofjudgment, an understandingof regulations,a knowledgeof science, a graspof compliance,and an appreciation of common practices. Sinceearly2000,Ihavealsobeeninvolvedwithseveraltrainingopportunitiesand I struggled to ?nd good, concise, practical resources, one of which I could just hand to a new scientist who wishes to gain a greater understanding of stability sciences. In addition, I encountered the same questions posted over and over on different stability best practices discussion forums. As a book lover, I also have a good collection of technical books. Unfor- nately, most of the stability related volumes are outdated. Many of these materials are theoretical and do not contain much practical information. I understand that the pharmaceutical industry during this period is quite volatile, and guidelines are changingrapidlywhileregulatoryagenciesareworkingcloselywiththepharmac- tical industryto accommodatethese changes;however,thefundamentalinformation continues to remain quite the same, just as current Good Manufacturing Practices (cGMP) continue to be the standard industry practice. Therefore, I hoped to ass- ble a practical handbook to ?ll this void.