SURVEY: Medical Device Regulation (MDR) for European Innovators
The objective of this survey is to capture the consequences of the Medical Devices Regulation (MDR) on innovative European companies, including those that have received significant government money. We expect that a contradiction could emerge between the massive investment done by the EU and Member States and the consequences of MDR.
This survey is intended for:
- EUCOPE members
- France Biotech members
- MedTech companies (with EU operations)
Please feel free to forward this survey to your regulatory and financial departments.
Disclaimer – confidentiality – your answers will remain confidential, collected by EUCOPE and France Biotech ; no individual data will be published.
The European Confederation of Pharmaceutical Entrepreneurs (EUCOPE) is Europe’s trade body that gives a bigger voice to small and mid-sized innovative companies working in the field of medical technologies and pharmaceuticals.
France Biotech is an independent association that brings together France leading innovative health companies and their expert partners. As a leader in health innovation and a privileged intermediary with public authorities in France and Europe, our mission is to support the development of this industry.