Digitalizing lifecycle processes in the Medical Device Industry with inspiring solutions

 

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.

 

 

 

At this webinar, Rick Stroot, Senior Application Engineer, will provide some insights on how the decline in innovation can be turned around by using some inspiring solutions that will:

• Speed up documentation creation and regulatory process compliance
• Enable easy reuse of information in different processes and documents
• Supports completeness of required information
• Allow visualization of dependencies between single data sets instead of references to documents

 

Details

 

What

Live Webinar: Digitalizing lifecycle processes in the Medical Device Industry

 

When

Thursday, April 25, 2024

 

Where

Online

 

Time

14:00 - 14:45 hr CEST