January/February 2017

Biopharma Asia

January/February 2017 | Volume 6 Issue 1


Modernizing Biopharmaceutical Manufacturing: From Batch to Continuous Production

Robert Dream, Managing Director HDR Company LLC


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

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


Pyrogen Testing in the 21st Century

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


Points to Consider for the CMC Development of Therapeutic Biologics

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


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

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