By Bhavya H M, Sr. Executive, Business development, TÜV Rheinland India

TÜV Rheinland LGA Products GmbH is now a notified body for the EU Medical Device Regulation (MDR) 2017/745 / Introduction of Eudamed central database / Increased requirements for notified bodies.

Device manufacturers are usually familiar with proper design methods for devices, but often get lost navigating through the standards and regulations necessary for developing wireless medical ...

Since the discovery of radiation and radioactivity more than 100 years ago, radiation protection standards and the philosophy governing those standards have evolved. Proper evaluation of these ...