I am responsible for the following;-Taking part in the MDR Transition Project as the MDR Team Administrator in the team responsible for ensuring compliance with the legislation-Preparation of biological evaluation files of all products and coordination of the biological evaluation process -Monitoring and Evaluating Major & Minor Changes according to legislation-Updating of relevant procedures,-Preparation of MDR compliant technical files -Reflecting product changes to the technical documentation-Updating Risk management files-Tailoring and organizing the certification of products-Taking an active role in internal¬ified body audits