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20160128 EGA Regulatory and Scientific Affairs Conferenc

Position Paper. Reference safety information: challenges to the generic industry due to labelling harmonisation issues among different Member States

8 May 2020

Policy

Open

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

10 April 2020

External Resource

Open

Position Paper. Incentives Review The Orphan and Paediatric Incentives

1 March 2020

Policy

Open

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

30 January 2020

Report

Open

Medicines Shortages: Causes and Recommendations

17 January 2020

Infographic

Open

AMR Industry Alliance 2020 Progress Report

16 January 2020

Report

Open

Perceptions and recommendations of physicians/KOLs on value added medicines

21 November 2019

Report

Open

The secret to improve access to value added medicines

14 November 2019

Policy

Open

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

Report

Open

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