Introduction to EU Medical Device Regulation (MDR): Key Terms
European Union Medical Device Regulation (EU MDR) 2017/745 is a framework governing safety and performance of medical devices in EU. It came into full effect on May 26, 2021, replacing the previous Medical Device Directive (MDD). It aims to address gaps in oversight...
How to Avoid Medical Device Product Recalls? 8 Strategies
Medical device product recalls are part of regulatory oversight for ensuring the best quality devices are available in the market. Getting notified by regulatory authorities for product recall will tarnish the medical device manufacturer’s image. Hence, we have...
7 Benefits of Risk Management in Medical Device Production
Risk management in medical device production is a systematic, dynamic, continuous, and multifaceted process. In this highly competitive medical device landscape, implementing risk management strategies is not only about compliance but also a necessity. Manufacturers...