Pharmaceutical Industry Practices on Genotoxic Impurities

Author:   Heewon Lee (Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, USA)
Publisher:   Taylor & Francis Inc
Volume:   107
ISBN:  

9781439874202


Pages:   536
Publication Date:   29 August 2014
Format:   Hardback
Availability:   In Print   Availability explained
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Pharmaceutical Industry Practices on Genotoxic Impurities


Overview

A great deal of confusion and uncertainty over genotoxic impurity (GTI) identification, assessment, and control exists in the pharmaceutical industry today. Pharmaceutical Industry Practices on Genotoxic Impurities strives to facilitate scientific and systematic consensus on GTI management by presenting rationales, strategies, methods, interpretations, practices, and case studies from the pharmaceutical industry. Featuring the contributions of industry leaders from nine major pharmaceutical companies, this authoritative text: Explores the safety, quality, and regulatory aspects of GTIs Provides an overview of the latest FDA and EMEA guidelines Explains the how and why of various GTI control tactics and practices Describes genotoxicity evaluation, acceptable exposure calculation, and analytical methods for testing Includes real-life examples of GTI control in drug substance and drug product development processes Containing case studies from large and small pharmaceutical firms in multiple geographical regions, Pharmaceutical Industry Practices on Genotoxic Impurities supplies an overview of—and a current framework for—GTI control in the pharmaceutical industry, demonstrating how proper management of GTIs can occur with the appropriate guidance, a firm grasp of the practical implications, and effective information sharing between disciplines.

Full Product Details

Author:   Heewon Lee (Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, USA)
Publisher:   Taylor & Francis Inc
Imprint:   CRC Press Inc
Volume:   107
Dimensions:   Width: 15.60cm , Height: 3.30cm , Length: 23.40cm
Weight:   1.150kg
ISBN:  

9781439874202


ISBN 10:   1439874204
Pages:   536
Publication Date:   29 August 2014
Audience:   Professional and scholarly ,  College/higher education ,  Professional & Vocational ,  Tertiary & Higher Education
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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Author Information

Heewon Lee is Senior Associate Director of the Chemical Development Department at Boehringer-Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, USA. She is also leader of the Analytical Research Group, an active participant in the Genotoxic Impurity Council, and a member of the Pharmaceutical IQ Consortium Working Group. She holds a BS and a MS from Seoul National University, South Korea, as well as a Ph.D from the University of Michigan, Ann Arbor, USA. Previously, she worked at ArQule, a biotechnology company located in Woburn, Massachusetts, USA. After ArQule, she joined the Medicinal Chemistry Department at Boehringer-Ingelheim before moving to her current position.

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