Toronto, Canada (PRWEB) March 05, 2013
The expiration of patents and other intellectual property rights for originator biologics over the next decade opens up opportunities for biosimilars to enter the market and increase competition. Despite the challenges associated with biosimilar drug development, many drug manufacturers are entering the race to develop biosimilars — especially for blockbuster mAbs. With increased clinical trial activity through Phase III, the ability to recruit patients into these important studies becomes a key stepping stone to Biosimilar commercial success.
Join our speaker, Rodeina Challand, Executive Director of Biosimilars Development at PRA , for an in-depth look at the challenges and solutions in conducting biosimilar trials.
A Q&A with the audience will follow the main presentation.
For more information about this event or to register, visit: http://xtks.in/xto565-event
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Karen Lim (416) 977-6555 ext 227