by April Breyer Menon | Jun 15, 2020
Based on an announcement last week, the longtime generics manufacturer Lannett would become among the first to file for insulin glargine product approval under the 351(k) Biologics License Application pathway. Venable’s Ha Kung Wong discusses previous and future...
by April Breyer Menon | Jun 8, 2020
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by April Breyer Menon | Jun 7, 2020
Despite the United States having had a biosimilar pathway for a decade now, the industry has launched just 17 biosimilars, well behind the pace in Europe and India. Several pieces of legislation have been introduced in Congress to help boost uptake, generate savings...
by April Breyer Menon | Jun 4, 2020
In an extended interview with the Center for Biosimilars, Venable’s Ha Kung Wong and April Breyer Menon discussed potential biosimilars legislation, including the Hatch-Waxman Integrity Act, Stop STALLING Act, Biologic Patent Transparency Act, Affordable and...
by April Breyer Menon | May 28, 2020
It’s no secret that the US biosimilar industry has had a slow start in terms of uptake. Although the Hatch-Waxman Act and the Biologic Price Competition and Innovation Act (BPCIA) established pathways to approval for both generic drugs and biosimilars, there is still...