Nowadays, all companies active in the life science ecosystem consider data as a crucial asset to their success. Pharma companies are collecting more and more information during their clinical trials or commercial and medical activities. Clinical laboratories have to...
Regulation (EU) 2017/745 on medical devices (MDR): our recommendations to getting the most out of the extended transitional period
The European Medical Device Regulation (MDR), which came into force on May 26, 2021, tightens the requirements for obtaining CE marking, for both products already marketed in the European Union and for new and future products. The substantial changes it introduces, to...