Rajasree PH Nair

Supporting Clinical Affairs and Regulatory Affairs activities for medical devices in an EU-MDR-regulated environment. Contributing to clinical literature reviews, evidence appraisal, and scientific documentation for clinical evaluation activities. Assisting in the preparation and maintenance of Clinical Evaluation Reports (CER), PMS, PSUR, and PMCF documentation. Gaining practical exposure to EU-MDR requirements, regulatory documentation, post-market activities, and product lifecycle processes. Supporti