SMART-TRIAL provides Medtech with answers to the Medical Device Regulation
A unique opportunity to gain insights on how Surveys can help fulfil the requirements on Post-Market Clinical Follow-Up (PMCF) under the new EU Medical Device Regulation (MDR)Clinical Data Experts SMART-TRIAL announced a unique online Q&A session where MedTech clinical teams are encouraged to ask questions about using surveys for Post-Market Clinical Follow-up (PMCF), to comply with the EU Medical Device Regulation (MDR). Participants can submit their questions before and during the live event which is scheduled for