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Formal Meetings with FDA for Biosimilar Products

by Frank Sorce | Feb 10, 2016 | Blog, Drug Development Consulting, Gilbert “Chip” W. Carnathan, Regulatory Affairs

February 10, 2016 | Chip Carnathan, PhD, RAC, Director Regulatory Affairs | Regulatory Affairs, Drug Development Consulting Yeah, yeah, we know. The general public considers biosimilars to be “generic” versions of approved biological products. The FDA has gone to...
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