Preparing your Quality Management System for the MDR: QA Best Practices
RS-Ness supports Life Science companies in QA, Regulatory Affairs, Clinical affairs, Validation and Project Management.
We will assist you with an MDR gap assessment to help you create an appropriate project plan, and support the transition throughout the Regulatory, Clinical, QA, Validation, and Engineering processes.
Our clients range from small Start-Ups to international companies.
If you have any questions, or if you need professional support, please contact us.
