In our first post on literature reviews for medical device clinical evaluation reports (CERs), we looked at the importance of multiple databases and using refined, comprehensive search strategies to...
EU MDR
EU MDR Literature Reviews – best practice for database selection and search strategies
The EU’s Medical Device Regulation (MDR) 2017/745 raises the bar for device manufacturers looking to stay compliant. With its introduction into law now postponed to May 2021, device manufacturers...
EU Medical Device Regulation: What does it mean for manufacturers?
Updated: On 24 April 2020, in the Official Journal of the European Union, the EMA confirmed a one-year postponement to the go-live date for the EU Medical Device Regulation and an extension of...
