The Essential EU Medical Device Regulation Toolkit

Medical device manufacturers need to comply with the EU Medical Device Regulation (MDR) in order to sell within the EU market. From May 26th 2021 they will be required to establish a comprehensive risk-based Quality Management System (QMS). Download our free toolkit which will help you achieve MDR compliance.

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The Toolkit Includes

  • Checklist

    Check off the steps you need to take to ensure your organisation is prepared for the new regulation.

  • White Paper

    Learn how manufacturers can implement a quality management system that meets the requirements of MDR.

  • Customer Insights

    Find out how our software has revolutionised Omega Diagnostics’ processes to help them achieve Quality, Safety and Regulatory excellence.