This webinar from HCWH Europe covers the provisions laid out in the Health Technology Assessment and how they relate to the MDR.
This webinar outlines the current regulatory framework applicable to medical devices, including the state of the European Database on Medical Devices (EUDAMED), which is due to become operational in 2019.
Oliver Bisazza from industry association MedTech Europe addresses the challenges, concerns, and opportunities that the new MDR represents for the industry. Whilst Tomas Delimon representing Zorgnet-Icuro, the Flemish healthcare provider and HCWH Europe member, outlines the approach they are taking to incorporate environmental sustainability, as well as quality and safety concerns in their medical devices procurement.
Read more: www.bit.ly/2OaLDdw
