European Commission initiative to improve patients' understanding of biosimilar meds

23 January 2017

Today, the European Commission published a unique Q&A for patients with reliable information on biosimilar medicines.

Stakeholders value these efforts to provide unbiased, scientifically correct and yet easy to understand information on biosimilar medicines through the Q&A on Biosimilar Medicines, now available in seven EU languages.

This consensus information on biosimilar medicinal products was drafted for patients together with the European Medicines Agency, the European Commission and relevant stakeholders: the European Patients Forum (EPF), the European Federation of Crohn's & Ulcerative Colitis Associations (EFCCA), the Standing Committee of European Doctors, European Federation of Pharmaceutical Industries and Associations (EFPIA), European Association for Bio-industries (EuropaBio) and Medicines for Europe.

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