Create and maintain plans and reports for regulatory authorities, including Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), Post-Market Clinical Follow-up Plans (PMCF-P), Post-Market Clinical Follow-up Reports (PMCF-R), Summary of Safety and Clinical Performance (SSCP), Periodic Safety Update Reports (PSUR). Collaborate closely with cross-functional teams to ensure the timely delivery of high-quality clinical evaluation reports (CERs) and related documents.