Value Added Medicines: Time to Adjust the HTA Decision Frameworks

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

The Benefits of Biosimilar Medicines

Join Medicines for Europe – 2017

Global Healthcare Trends and Outlook

Medicines for Europe Country Specific Market Access Policies

The Impact of Biosimilar Competition in Europe

Tweetup with Jacek Glinka | Friday 24 March 2017 | 10.00 – 10.45 (CET)

15th Biosimilar Medicines Conference

BIOSIMILAR MEDICINES: A GAME CHANGER FOR HEALTHCARE SUSTAINABILITY

Friday 24 March 2017 | 10.00 – 10.45 (CET)

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