The Evolving Landscape of Medical Device Regulatory Approvals in 2025
This blog will discuss recent trends and changes in regulations for medical devices, highlighting the accelerating approval pathways such as FDA 510(k), PMA, and de novo routes. It will emphasize the importance of staying updated with evolving standards worldwide, especially focusing on the European Union’s Medical Device Regulation (MDR) and AI-related regulations, which are reshaping the compliance … Read more