Solutions for Medical Devices Digital Technical Publications

The implementation of the new Medical Device Regulation (MDR), the In-Vitro Diagnostic Regulation (IVDR) and the Unique Device Identification (UDI) is the key challenge for medical device manufacturers along with the growing pressure of cost reduction and high demand for innovation.

Our state-of-the-art, ready-to-use infrastructure and dedicated Center of Excellence (CoE) with 1000+ engineers support the technical publications delivery with operational cost savings and improved customer services for our clients.