Ready for MDR
8 reasons why an integrated ERP software is indispensable when implementing the MDR
Consistent risk and quality management system, complete traceability, consideration of the entire product life cycle, EUDAMED upload and much more: The European Medical Devices Regulation (MDR) places numerous regulatory requirements on medical technology companies and their quality management. The "qualified person" (Art. 15) is personally responsible for compliance with the regulatory provisions.
In this white paper you will find out how you can map the requirements of the MDR securely and conveniently with integrated ERP software.
These requirements can no longer be mapped with Excel and paper alone. Integrated ERP software provides a remedy: it monitors processes, networks company areas, prepares information, avoids data silos and reduces the error rate.
Find out from eight fields of action with many practical examples how you can successfully implement the requirements of the MDR in your company with integrated ERP software.
This white paper explains:
- How integrated ERP software supports quality management and the qualified person in MDR implementation
- Which relationships you can recognize and analyze with system-based ERP software
- What a previously untapped potential your data has
- How to reduce the administrative effort required to comply with the MDR regulations
- The advantages of not using isolated solutions
- How intelligent workflows and automated processes in ERP ensure more compliance
