Generic Drug Product Development

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Generic Drug Product Development

International Regulatory Requirements for Bioequivalence

Manufacturing industries Biology, life sciences Engineering: general Pharmaceutical chemistry and technology

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Language: English

Published by: CRC Press

Published on: 19th April 2016

Format: LCP-protected ePub

ISBN: 9781040169001


Introduction

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing.

Regulatory Requirements

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.

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