[Panel 5] International Issues in Biopharma Patent Litigation

Date: 
Tuesday, November 19, 2019 - 3:00pm to 4:15pm
Panel Description: 

Biologic and pharmaceutical patent litigation differs from other types of patent litigation in significant ways. Biopharma litigation are frequently the result of statutory provisions for resolving patent disputes that are part of the generic drug or biosimilar approval framework. These provisions create unique substantive and case management issues. Where innovative biologic and pharmaceutical products requiring first-time FDA approvals are involved, other unique legal and case management issues often arise. Biologic and pharmaceutical patent litigations also frequently call on courts to balance the public’s interest in encouraging and rewarding the discovery and development of new drugs and biologics against that of making differentiated, life-altering, and/or lifesustaining therapies available to patients who may benefit from them. Topics include small molecules, generic pharmaceuticals, biologics, biosimilars, PTEs, and SPCs.

Moderator

Crowell & Moring LLP

Washington, D.C., USA

Dialogue Leaders

High Court of Justice of England and Wales

London, United Kingdom

Sandoz

Princeton, NJ, USA

Davè Law Group, LLC

Alexandria, VA, USA

MorphoSys AG

Munich, Germany

Darts-ip

Lille, France