eVisit Patient Reported Outcomes (ePRO)
Improve the ability of patients to enter data and the accuracy of clinical trial data

eVisit(ePRO) effectively solves the problems of difficult information acquisition, poor compliance, and difficult handling paper reports of patients in traditional clinical trials. Patients can enter information anytime and anywhere via eVisit mobile terminal to realize real-time data upload and patient information management, effectively improve the accuracy of research data, strengthen the communication between doctors and patients, and effectively promote the progress of clinical trials.

System Features

 electronic informed consent

Set up informed consent templates by site

Patients report

Patients report
Pictures captured
Data synchronization

Follow-up reminder

Doctor-subject communication

eVisit APP——Easier access to patient’s data