The Essential Medical Device Regulation Toolkit

Download our toolkit which will help you comply to the mandatory MDR coming into effect May 26th 2020. Medical device manufacturers need to comply in order to sell within the EU market and will be required to establish a comprehensive risk-based Quality Management System.

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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.