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20160128 EGA Regulatory and Scientific Affairs Conferenc

Policy Roadmap for Medicines Manufacturing Leadership

6 July 2020

Policy

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Call for tenders SANTE/2020/C3/29 for the supply of medicinal products used for intensive care patients subject to the novel coronavirus (COVID-19) disease – policy and technical concerns

25 June 2020

Policy

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Preparing for a potential second COVID-19 wave. Joint statement by Medicines for Europe and EFPIA with Kearney

22 June 2020

Policy

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LESSONS LEARNED FROM COVID-19 – POLICY PAPER

22 June 2020

Policy

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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

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

29 October 2019

External Resource

Unofficial Ukrainian translation (PDF/600 KB) (PDF/600 KB) English (PDF/1.85 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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