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Biosimilars: What the Communicator Should Know About This Growing Field

Presenters

Lawrence  Liberti, PHD, RAC

Lawrence Liberti, PHD, RAC

Director, D.K. Kim International Center for Regulatory Science, The Kim Center/ USC DRQS, United States

Dr Liberti has worked in pharmaceutical regulatory affairs, communications and clinical R&D for the past four decades. From 2009 to 2021 he served as the Executive Director of CIRS. He is the Director of the DK Kim International (USC DRQS) and has been actively involved in promulgating best regulatory practices especially in the emerging markets. He received his doctorate in International Regulatory Policy through the WHO Collaborating Centre for Pharmaceutical Policy and Regulation, Utrecht University, where his research centered on expedited regulatory pathways. He is a volunteer with the nonprofit Erudee Foundation.

Matthew  Frankel, MD, MBA

Matthew Frankel, MD, MBA

Executive Director, Medical Affairs Biopharmaceuticals North America, Sandoz Inc., United States

Eileen  Girten, MS

Eileen Girten, MS

Medical Writing Therapeutic Area Lead, Pfizer, United States

Eileen M. Girten serves as the Medical Writing Therapeutic Area Lead at Pfizer and brings nearly 17 years of medical writing experience spanning publications and regulatory documentation. She holds a Bachelor of Arts in Chemistry from Rosemont College, a Master of Science in Psychology from Saint Joseph’s University, and a Master of Science in Biomedical Writing from the University of the Sciences in Philadelphia (currently Saint Joseph’s University). Ms. Girten is located in New Jersey.

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