Live Webinar April 25: Digitalizing Lifecycle processes in the Medical Device Industry

The medical technology sector is one of the most innovative industries in the world, but the innovative strength of manufacturers is constantly being slowed down by ever-increasing regulatory requirements. The European Medtech industry has a decline in innovation due to too complex regulatory system for medical devices (MDR/IVDR) and a digitalization that is far too slow with a lack of data usage. Proof of the regulatory compliance of a medical device is provided on the basis of the technical documentation, which is the result of the product development process and various interface processes.

If regulatory requirements are not fulfilled, manufacturers cannot sell products and therefore cannot operate successfully in economic terms.

Join us at this free webinar Thursday April 25, 2024 and learn how we can enable more innovation.