ESRA BARUT

Esra Barut is a dedicated and detail-oriented professional with over 8 years of experience in Post-Market Surveillance within the medical device industry. Post Market Surveillance works with a product/medical device before ideation till after it is on the market and analyzes existing historical data to evaluate and monitor the performance of launched products. Over the years Esra Barut has developed a strong foundation on the EU Medical Device Regulations (EU MDR) and has worked extensively on key deliverables such as Periodic Safety Update Reports (PSURs), Clinical Evaluation Reports (CERs), and Post-Market Surveillance Plans and Reports.

Esra is passionate towards evaluating the performance of medical devices and for the opportunity to contribute to the ongoing safety and effectiveness of medical devices that impact patients' lives. Esra enjoys working cross-functionally and applying both analytical thinking and regulatory insight to ensure compliance while supporting innovation and product improvement.