Biopharma Asia

January/February 2017 | Volume 6 Issue 1

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Modernizing Biopharmaceutical Manufacturing: From Batch to Continuous Production

Robert Dream, Managing Director HDR Company LLC

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Enhancing Compliance through Novel Approaches to Commissioning & Qualification/Valida...

Brian Urban, Associate Director, Quality Systems and Enterprise Management, Corporate Qua...

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Pyrogen Testing in the 21st Century

Ingo Spreitzer, Deputy Head Division Microbiology, Section 1/3 “Microbial Safety”, Pa...

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Points to Consider for the CMC Development of Therapeutic Biologics

Willie Wilson III, Ph.D., Primary Product Quality Reviewer Office of Biotechnology Produc...

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From Development to Validation: Analytical Method LCM and its Associated Challenges

Natasha Shanker, Ph.D, Associate Director Biologics Development Center, Dr. Reddy’s Lab...

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