Regulatory news related to digital documentation for medical devices
Shifting your supplier status to comlpy with EU-MDR is a approach for former OEM constelations.
Last year, our CEO Michael was interviewed by the notified body TÜV Rheinland on the subject of digitalization. The topic is more relevant than ever.
GSPR Management and the process you need to follow.
How to shift from MDD Essential Requirements to Medical Device Regulation General Safety and Performance Requirements
eTD and eQMS solution for medical devicesMade in Germany