While the deadline for EU MDR is fast approaching, creating and maintaining Clinical Evaluation Reports won't stop on the 26 May 2021. Even if you're compliant by that date, having an efficient and...
EU MDR
How to make EU MDR CER literature reviews more efficient
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 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...
