Registration is open for the next training course on the Medical Devices Regulation (MDR)
SFL is pleased to present at a new training course organized by the Medtech & Pharma Platform (MPP), entitled “Overview of Medical Devices Regulation and Workshop on Clinical Evaluation” (28th March, 2019, Basel). The course will focus on changes in responsibilities and requirements to comply with the MDR that is replacing the existing Medical Device Directive (MDD) legislation. Furthermore, the course will include a workshop on practical elements to consider in completing a clinical evaluation of devices according to the new MDR. The MDR will come into full effect in spring of 2020.
Registration can be done here.