Discuss the commercial, clinical and regulatory viability of developing a biosimilar with experts such as:
| Philippe Stas |
Chief Operating Officer |
ALGONOMICS |
| Alan Colley |
Senior Regulatory Affairs Manager |
AMGEN |
| Raja Velagapudi |
Director, Pharmacokinetics and Bioequivalence |
BARR LABORATORIES |
| Louis Christian Clauss |
Director of New Product Development |
BAXTER INTERNATIONAL |
| Cornelia Ulm |
Head of Regulatory Affairs and Quality Assurance |
BIOPARTNERS |
| Helmut Brunar |
VP Research & Business Development, Biosimilars |
KWIZDA PHARMA |
| Andrea Rappagliosi |
VP Health Policy & Market Access |
MERCK SERONO |
| Henning Blume |
CEO |
SOCRATEC R&D |
| Jay Madan |
Vice President, Business Development Biopharmaceuticals |
RELIANCE LIFE SCIENCES |
| Harald Sitte |
Institute of Pharmacology |
MEDICAL UNIVERSITY VIENNA |
| Asterios Tsiftsoglou |
Professor, Pharmocognosy-Pharmacology |
ARISTOTLE UNIVERSITY OF THESSALONIKI |
| Ivan Cohen-Tanugi |
Vice President, Global BioGenerics, Portfolio,
Strategy & Marketing |
TEVA EUROPE |
| Murali Tummuru |
CEO |
VIRCHOW BIOTECH |
| Hemanth Nandigala |
Executive Director, Commerce |
VIRCHOW BIOTECH |