Responsible for ensuring MDR compliance for all MDR-classified devices and supporting legacy MDD devices with post-market surveillance and vigilance until they are fully phased out. Including conformity checks, technical documentation is up to date and meets MDR Annex II and III. Post-market surveillance (PMS) is conducted per MDR Article 83. Reporting obligations for serious incidents and field safety corrective actions (FSCA) under MDR Article 87. Including compliance with UDI, registration.