Webinar: Recent legislative developments affecting biologics and biosimilars

June 2019

Many of the top-selling drugs worldwide are biologics, and several companies are seeking to produce biosimilars to compete in these lucrative markets.

Recently, a flurry of proposed legislation has threatened to drastically alter the US regulation of and policies on wide ranging topics such as drug pricing, mandatory licensing, patent thickets, and the availability of post-grant proceedings.

Session 2 of our 2019 biosimilars webinars series focuses on key factors decision makers need to be aware of when considering currently pending legislation, including:

  • Key provisions of proposed legislation.
  • European perspectives and approaches to similar issues.

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Contributing authors

Matthew Royle, Evelyne Friedel, Judith Krens and external speakers: Heather M. Schneider , Michael W. Johnson and Tara L. Thieme (Willkie Farr & Gallagher LLP)