Industry Insight: Modernizing Medtech Regulatory Affairs

Medtech regulatory leaders are harmonizing regulatory processes across divisions and geographies, according to the MedTech Regulatory Benchmark Report. While the shift to streamline regulatory operations in the medical device and diagnostic industry is underway, the study shows companies must do more to eliminate manual processes, drive speed, and meet evolving regulations like EU MDR and IVDR.

Infographic by Veeva MedTech illustrating medical device and diagnostic industry progress towards regulatory modernization