Reeshav Pradhan

My role is to develop a concept and prototype of a collaborative tool for Post-Market Surveillance that addresses the key weaknesses of today's process and to enable manufacturers to improve their post-market surveillance activities with respect to documentation quality, readability and avoidance of inconsistencies throughout the technical documentation of the medical device and especially to improve reaction time and seamless integration of complaint handling with preventive and corrective action.

Regulatory Affairs, Healthcare Management System, Medical Technology, Medical Electronics