We are proud to welcome MedTech Europe as a member of the EU4MEDTECH Stakeholders Forum!
As the leading European trade association representing medical technology industries – from diagnostics, medical devices and digital health – MedTech Europe plays a central role in shaping health innovation policy across Europe. With its broad membership base and deep expertise in policy and regulatory affairs, digital health, and market access, MedTech Europe is an essential partner in discussions about the future of medical device (MD) and in-vitro diagnostics (IVD) regulation.
“We’re pleased to support EU4MEDTECH’s efforts to provide practical tools to strengthen the regulatory science behind clinical and performance evaluation of medical devices and in vitro diagnostic medical devices,” said MedTech Europe Director of Regulatory Affairs Petra Zoellner. “A future-fit legal framework must be efficient, predictable, and innovation-friendly. One that ensures patient safety while enabling timely access to technologies across Europe. We look forward to contributing our expertise to help co-create solutions that work for patients, health systems, and innovators alike.”
Their involvement in the Stakeholders Forum marks a significant milestone and strengthens EU4MEDTECH’s ambition to develop smarter, evidence-based, and innovation-supportive regulatory approaches. Engaging key players like MedTech Europe helps ensure that the project outputs are relevant, feasible, and aligned with the realities of the MedTech sector.
Join the Conversation
The EU4MEDTECH Stakeholders Forum is a growing network that brings together regulators, industry experts, researchers, clinicians, and policy leaders to co-create practical tools, provide feedback on project outputs, and contribute to smarter, more adaptive regulation.
If you’re involved in medical technology, regulation, research, or healthcare, we warmly invite you to take part in the EU4MEDTECH Stakeholders Forum. Become a member, stay informed and Get Involved!
