Today, experts from the Biomedical Alliance in Europe (BioMed Alliance) are advising the Joint Research Centre (JRC) of the European Commission in Ispra, Italy, on the clinical evaluation of high-risk medical devices. Representatives of the healthcare professions will discuss how scientists and clinicians can help to implement the new EU Medical Devices Regulation (MDR) and the new EU In Vitro Diagnostic Medical Devices Regulation (IVDR).

Read the press release here

We use cookies to improve your experience on our website. By browsing this website, you agree to our use of cookies.