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Hyatt Regency Bethesda

2013年11月13日 (水) 午前 7:15 - 2013年11月14日 (木) 午後 4:30

One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814-5326

DIA Biosimilars 2013

Commercialization

Session Chair(s)

David  Gaugh, RPH

David Gaugh, RPH

Senior Vice President for Sciences and Regulatory Affairs

Generic Pharmaceutical Association (GPhA), United States

During this session, government and industry experts, from a broad range of backgrounds and experiences, will provide in-depth overviews on substitution and interchangeability and on naming and labeling as they relate to the biosimilar market. Experiences from the European biosimilar market as well as other non-US regulated markets will be incorporated to provide overviews.

Speaker(s)

Gillian  Woollett, PHD, MA

Interchangeability & Substitution

Gillian Woollett, PHD, MA

Samsung Bioepis, United States

Vice President, Head Regulatory Strategy and Policy

Steve  Miller, MD

Interchangeability & Substitution

Steve Miller, MD

Express Scripts, United States

Senior Vice President & Chief Medical Officer

Thomas  Felix, MD

Interchangeability & Substitution

Thomas Felix, MD

Amgen Inc., United States

Medical Director, R&D Policy, Global Regulatory Affairs and Safety

Erika F. Lietzan, JD, MA

Naming & Labeling

Erika F. Lietzan, JD, MA

University of Missouri, United States

Associate Professor of Law

Joerg  Windisch, PHD

Naming & Labeling

Joerg Windisch, PHD

Sandoz Biopharmaceuticals, Austria

Chief Science Officer

Panel  Discussion

Panel Discussion

All Session Speakers, United States

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