Generic Drug Product Development Generic Drug Product Development

Generic Drug Product Development

International Regulatory Requirements for Bioequivalence

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    • $89.99

Publisher Description

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutica

GENRE
Professional & Technical
RELEASED
2016
April 19
LANGUAGE
EN
English
LENGTH
332
Pages
PUBLISHER
CRC Press
SELLER
Taylor & Francis Group
SIZE
3.8
MB
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