Mirza Suhel Haque

Associate @Wipro

Kolkata, IN

Reviewed and processed medical device adverse event reports.• Assessed case validity, seriousness, and expectedness.• Ensured compliance with regulatory guidelines (e.g, CDSCO, EU MDR, FDA).• Performed follow-ups for missing information.• Maintained accurate documentation in safety databases.• Assisted in signal detection and risk management activities.• Coordinated with quality, regulatory, and clinical teams.