US FDA Advisory committee hears first-hand about the decade of EU experience with biosimilar medicines use

Medicines for Europe Director General Adrian van de Hoven participated in the Open Public Hearing (OPH) of the July 13, 2017 Oncologic Drugs Advisory Committee US FDA Advisory Committee involving biosimilar medicines on 13 July 2017.

Letter from European and UK Life Sciences Organizations Underlining the Importance of Securing Ongoing Cooperation Between the UK and EU on Medicines

Position Paper External Reference Pricing for Generic and Biosimilar Medicines

Medicines for Europe Country Specific Market Access Policies

ISPOR 2016 EU – Value Added Medicines

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Healthcare System Inefficiencies Related To Medicines: Any Potential Room For Improvement?

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Value Added Medicines: The Need to Establish One Common Terminology for Repurposed Medicines

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Value Added Medicines: What Value Repurposed Medicines Might Bring to Society?

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Obstacles for Adoption of Value Added Medicines: Call for Policy Changes for Value Recognition of Repurposed Medicines

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Essential Medicines for Universal Health Coverage

Medicines for Europe’s Contribution to WHO’s Biological Qualifier (BQ) Developments (PRESENTATION and SPEECH)

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18 October 2016
Suzette Kox
Senior Director International
Biosimilar Medicines Group

Understanding the Science of Extrapolation and Defining Interchangeability – Dr. Elena Wolff-Holz, EULAR Symposium London

Value Added Medicines: Rethink, Reinvent & Optimize Medicines, Improving Patient Health & Access

EGA-EBG Summary Position Regarding the WHO Biologic Qualifier Proposal (INN Working Doc. 14.342)

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