GoBroad Clinical Research Center provides clients the service of medical monitoring during the clinical trial conduct. We develop Medical Monitoring Plan (MMP) and conduct medical monitoring for clinical trials, which help to secure the subject safety, improve the trial quality, and ensure the data integrity. Our main responsibilities include development of MMPs, subject eligibility review, protocol compliance review, medical review of individual and accumulated data and report, medical support to Data Monitoring Committees, medical review during data cleaning, medical coding review, participation in the development of PD management plan and PD definitions, review of protocol deviations and providing medical advice and solutions, and addressing other medical-related issues.