Conference - Princeton, NJ, United States
The session will focus on establishing the swiftest pathway for registration of Biosimilars in USAPast experiences of FDA regarding 10-20 year biologics approvals has paved the way to entry of biosimilars – therefore, a new paradigm is emerging, not only with an emerging new class of products but also a fresh Pharma and Regulator awareness of novel recombinant therapeutic proteins including monoclonal antibodies. Development strategies of a new generation of selective biologics including Biobetters are emerging. Also, Regulators worldwide now demand a higher quality standard of biologics.
Presented By: Dr. Hoss A Dowlat, RA, VP, Global Strategy, Pharma-Bio Consulting
Organization: Biopractice (http://www.biopractice.com/bioevents/)
Monday, 4th August, 2014 (09:00 AM - 05:00 PM)
NJHA Conference & Event Center
Princeton, NJ, United States
Contact: Gopal (firstname.lastname@example.org)
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