Ha Kung Wong discusses how the STRONGER Patents Act could affect biosimilars in a video for the Center for Biosimilars, Including changing inter partes review (IPR) burdens and claim construction standards to match those in district court litigations, standing in IPRs, and appeals of IPR institution decisions.
Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.
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