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20160128 EGA Regulatory and Scientific Affairs Conferenc

Did The 2017 Biosimilar Industry Pave The Way For A Productive 2018?

28 December 2017

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Value-added medicines: how repurposed medicines bring value to patients and pharmacists

21 December 2017

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Pharmacovigilance, traceability and building trust in biosimilar medicines

21 December 2017

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The associations representing the European and British life science industry (AESGP, ABPI, BGMA, BIA, EBE, EFPIA, EUCOPE, EuropaBio, Medicines for Europe, PAGB, Vaccines Europe) have today launched a joint policy document on the potential impact of the United Kingdom’s exit from the European Union

14 December 2017

Today, organisations representing the life science industry in the EU […]

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European Commission launches: “What I need to know about Biosimilar Medicines – Information for patients”, in 23 EU languages

29 November 2017

The European Commission launched today additional translations of the Q&A […]

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Europe’s life science industry urges the UK and EU27 to safeguard patients’ access to medicines with a clear transition period and a future cooperation agreement after Brexit

28 November 2017

The associations representing the European and British life science industry […]

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Medicines for Europe calls for greater cooperation on value added medicines to improve patient-centric innovation

22 November 2017

The 1st Value Added Medicines conference organised by the Value […]

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Medicines for Europe welcomes decision on EMA relocation to Amsterdam

21 November 2017

Medicines for Europe is very glad to see the Council […]

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Manufacturing cost transparency could combat pricing criticism, says expert

2 November 2017

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Commission sponsored study shows Supplementary Protection Certificate (SPC) Manufacturing Waiver will create Jobs, strengthen the pharmaceutical sector and reduce medicine costs

18 October 2017

On Thursday 12 October, the Directorate-general for Internal Market, Industry, […]

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