Performing Successful Clinical Evaluation Seminar
QUNIQUE will be hosting a new seminar discussing performing successful clinical evaluation in the medical device industry.
One of the major changes coming with the Medical Device Regulation (MDR) is the increased expectations on clinical data showing safety, performance, and benefit risk profile of a device when used as intended.
Devices that have been on the market for a long time will need to re-initiate clinical investigations if they do not have sufficient clinical data for the period they have been on the market.
Download this free white paper to find out more.