Woodcock Bemoans Lack Of 'Biobetter' Provision In BPCIA

CDER director lobbied for inclusion of a 505(b)(2)-like category for biologics, but it was ultimately not included in the 2010 legislation creating the biosimilar pathway; Woodcock urges patience on the development of the biosimilar marketplace and notes the agency will be keeping an eye on the development of biobetters, which are relatively new innovations.

Woodcock_Janet_1200x675
CDER Director Janet Woodcock discussed the future of the US biosimilars market.

More from Biosimilars

More from Biosimilars & Generics