Identify your potential MDR/IVDR deviationsfor 850 EUR per day!

PROSYSTEM is going to check your existing procedures, work instructions and templates to identify potential non-conformities against the requirements of the Medical Device Regulation / In-vitro-Diagnostic Regulation and will help you to understand the regulatory background of the requirements.
Additionally, opportunities for improvement will be highlighted to help you streamline processes and support the effectiveness in your business.The offer is limited from July to September 2018 and to 5 days max.

For questions or a quotation please contact us.