EUCOPE – the European Confederation of Pharmaceutical Entrepreneurs
Conferences and next Working Groups
- 4 February 2016: EUCOPE Orphan Medicinal Products Working Group Meeting in Brussels
- 22 February 2016: EUCOPE Pricing & Reimbursement / Market Access Working Group Meeting in Brussels
- 23 February 2016: EUCOPE Board Meeting in Brussels
- 15 March 2016: EUCOPE Regulatory / Pharmacovigilance / Medical Device Working Group Meeting in Brussels
- 21 June 2016: EUCOPE Board Meeting in Brussels
- 5 July 2016: EUCOPE Regulatory / Pharmacovigilance / Medical Device Working Group Meeting in Brussels
- 11 October 2016: EUCOPE Board Meeting in Brussels
- 15 November 2016: EUCOPE Regulatory / Pharmacovigilance / Medical Device Working Group Meeting in Brussels
European Biotechnology – A Medical Focus
EUCOPE is proud to be part of the 2015 publication “European Biotechnology – A Medical Focus” by Horn Publishing. Alexander Natz has contributed with a foreword on Biotechnology Innovation: The Impact of Clinical Trial Data Transparency. An online version of the publication can be found here.
EUCOPE provides a platform for discussion for pharmaceutical entrepreneurs. On a regular basis owners and CEOs of pharmaceutical companies and associations discuss solutions to improve the quality of life for patients and to strengthen the competitiveness of the European pharmaceutical industry.
The legal framework for pharmaceutical markets is set largely by the EU institutions. An active role in the political debate on the EU level is therefore more important than ever before. The early perception of future markets and reliable regulatory circumstances are key aspects for entrepreneurial success.
Knowledge about this legal framework and the active discussion and participation on the EU level is therefore essential for pharmaceutical entrepreneurs in order to generate innovations.
EUCOPE understands itself as service provider for its members. The association provides its members with an early understanding about regulatory developments.
Current regulatory topics are:
- EMA Transparency Policy (Policy 0700)
- Clinical Trials Regulation (Regulation (EU) No 536/2014)
- EMA Fees Regulation (Regulation (EU) No 658/2014)
- Commission proposal Review IVD legislation
- Commission proposal Review Medical Devices legislation
A tight monitoring and comprehensive information about future market conditions are valuable assets for entrepreneurial decisions. Questions such as access to finance, market access and reliable reimbursement conditions are of crucial importance for pharmaceutical entrepreneurs.
Please find out more about EUCOPE under About us.
EUCOPE in the News
EUCOPE is in regular contact with the press on current developments in the EU and national pharma markets.
Please find some examples here.