Biopharma Asia

March/April 2015 | Volume 4 Issue 2

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Supplier Qualification for Single-Use Technology

By: Scott M. Wheelwright, Co Founder and Principal Consultant Complya Asia Co., Ltd

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Low Endotoxin Recovery: An FDA Perspective

By: Patricia F. Hughes, Ph.D.,Team Leader in FDA/CDER in the Office of Pharmaceutical Qua...

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Analysing the Analytical Techniques for Counterfeit Drug Detection

By: Anna Luczak, Ph.D., Scientist Ravi Kalyanaraman, Ph.D., Associate Director Bristol-...

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Pharmaceutical Sourcing Strategies – An Indian perspective

By: Dr. Sanjit Singh Lamba, MPharm, PhD Managing Director, President-Global Brands Unit ...

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Trends and Opportunities in Pediatric Drug Development

By: Daniel E. Schaufelberger, Ph.D., Scientific Director and CMC Leader Janssen Research...

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The United States Pharmacopeia Addresses the Issue of Leachables and Extractables

By: Daniel Norwood, Distinguished Research Fellow Boehringer Ingelheim Pharmaceuticals, ...

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