MedTech Europe
Katalin Mate is a seasoned professional in regulatory affairs and industrial policy within the medical technology sector. Currently serving as Manager of Regulations & Industrial Policy at MedTech Europe since January 2017, Katalin oversees matters related to diagnostics, medical devices, and digital health for a diverse range of association members. Previously, Katalin held roles as Regulatory Affairs Manager and Regulatory Affairs Officer at the European Diagnostic Manufacturers Association from June 2010 to December 2016, and began a career in regulatory affairs as an Assistant at Bristol-Myers Squibb in Budapest from May 2007 to February 2010.
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MedTech Europe
MedTech Europe’s mission is to make innovative medical technology available to more people, while helping healthcare systems move towards a sustainable path. MedTech Europe encourages policies that help the medical technology industry meet Europe’s growing healthcare needs and expectations. It also promotes medical technology’s value for Europe focusing on innovation and stakeholder relations, using economic research and data, communications, industry events and training sessions. MedTech Europe started as an alliance in October 2012 formed by two organisations - EDMA, representing the European in vitro diagnostic industry; and Eucomed, representing the European medical devices industry. Promoting a balanced policy environment MedTech Europe engages with EU regulators, politicians and other decision-makers to help shape policies to promote innovation for our growing healthcare needs and expectations. Demonstrating the value of medical technology MedTech Europe promotes to its members and the wider industry value-based innovations that support more sustainable healthcare systems. We use economic research to show the benefits of medical technology and we organise many initiatives to explain the value we bring to healthcare systems in Europe. We bring stakeholders together to discuss trends, issues and opportunities.