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20160128 EGA Regulatory and Scientific Affairs Conferenc

Questions and answers on regulatory expectations for medicinal products for human use during the COVID-19 pandemic

10 April 2020

External Resource

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Why is Now the Right Time to Modernise the Eu Variations System?

30 January 2020

Report

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AMR Industry Alliance 2020 Progress Report

16 January 2020

Report

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Biosimilars in the EU – Information guide for healthcare professionals – now available in 23 languages

29 October 2019

External Resource

English (PDF/1.85 MB) (PDF/1.82 MB) Bulgarian (PDF/1.82 MB) (PDF/1.82 MB) […]

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Overarching recommendations for improved access to generic and biosimilar medicines in the hospital setting

7 October 2019

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Improving healthcare delivery in hospitals by optimized utilization of medicines

7 October 2019

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Positioning Statements on Physician-led Switching for Biosimilar Medicines

19 September 2019

Policy

Positioning Statements on Physician-led Switching for Biosimilar Medicines BIOSIMILAR MEDICINES […]

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Open letter to the Members of the European Parliament on the importance to sustain EU progress in fighting against antimicrobial resistance (AMR)

11 September 2019

Policy

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Medicines for Europe Commentary on the Draft EMA regulatory science strategy 2025

28 June 2019

Policy

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Annual Medicines for Europe and IGBA Conference 2019

4 April 2019

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