TM_002_MDR_rev 01

MDR (Medical Device Regulation (EU 2017/745)) is the new European regulation for medical devices. It replaces the MDD regulation.

At the end of the training, a questionnaire must be completed by the employee (hot evaluation).
If they obtain the training certificate, we consider that they are autonomous to carry out these tasks.
If you don't get enough points, further training will be organised with the responsible of this training.

No cold assessment is necessary.