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. This presentations will provide some insights on how this 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
Rick Stroot, InnoFour
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