MTE are pleased to announce the publication of the MedTech Europe 2024 Regulatory Survey Report and Executive Summary. This comprehensive report provides valuable insights into the current regulatory challenges faced by manufacturers under the In Vitro Diagnostic Regulation (IVDR) and Medical Device Regulation (MDR).
The findings highlight key concerns such as increased costs, regulatory unpredictability, and delays in conformity assessments, offering a critical look at the state of the regulatory framework and its impact on the industry.
You can access the full report and the accompanying executive summary via the public link: MedTech Europe 2024 Regulatory Survey: Key Findings and Insights – MedTech Europe
