Eu MDR Internal Audit Checklist: A comprehensive list of key compliance activities and criteria to ensure that a company has met all the relevant requirements under the European Medical Devices Regulation (EU MDR). The checklist covers activities such as validating design, system testing, risk management, post-market surveillance, and post-market clinical follow-up. It provides an invaluable way for organizations to audit their procedures and processes in order to confirm their compliance with EU MDR. An effective EU MDR Internal Audit Checklist ensures manufacturers remain compliant while producing products that are safe and reliable for all users.