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20160128 EGA Regulatory and Scientific Affairs Conferenc

US FDA Advisory committee hears first-hand about the decade of EU experience with biosimilar medicines use

13 July 2017

Policy

Medicines for Europe Director General Adrian van de Hoven participated […]

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Letter from European and UK Life Sciences Organizations Underlining the Importance of Securing Ongoing Cooperation Between the UK and EU on Medicines

13 July 2017

Policy

Open

Position Paper External Reference Pricing for Generic and Biosimilar Medicines

1 July 2017

Policy

Open

Medicines for Europe Country Specific Market Access Policies

23 May 2017

Policy

Open

Essential Medicines for Universal Health Coverage

7 November 2016

Policy

Open

Medicines for Europe’s Contribution to WHO’s Biological Qualifier (BQ) Developments (PRESENTATION and SPEECH)

18 October 2016

Policy

      18 October 2016 Suzette Kox Senior Director […]

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Understanding the Science of Extrapolation and Defining Interchangeability – Dr. Elena Wolff-Holz, EULAR Symposium London

10 June 2016

Policy

Open

EGA-EBG Summary Position Regarding the WHO Biologic Qualifier Proposal (INN Working Doc. 14.342)

21 March 2016

Policy

Open

Biosimilar Product Labelling

2 February 2016

Policy

Open

The value of generic medicines

26 November 2015

Policy

Read more about the value of generic medicines PDF version or […]

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