Regulatory Affairs Professional
Siemens Healthineers, United States
Masters in computer application.
18+ experience in software medical device industry.
prior and current experience include quality management, product risk management, complaints management and Regulatory affairs .
Published papers accepted in ECR 2022.
Consultant to various modalities on process and requirements for conducting clinical investigations/ multi reader studies for AI based devices .
develop strategies to clear AI based medical devices in various countries around the globe.
Author for various regulatory processes in the organization.
Member and contributor for various industry associations and AI committees - MITA / MDCI.
Disclosure information not submitted.
Thursday, May 11, 2023
13:45 – 14:45 CEST