Medrio offers solutions and support to pharmaceuticals, biotech, medical devices, and diagnostics, ensuring quality data capture and optimized workflows with CDMS/EDC, eCOA/ePRO, eConsent, and RTSM solutions.
A de minimis incentive was given to thank the reviewer for their time. The incentive was not used to bias or drive a particular response, nor was the incentive contingent on a positive endorsement. More Info
Clinical Research Coordinator in Research & Development at Rush University Medical Center (1001-5000 employees employees)
Pros
Ease of navigation for entering subject data.
Very organized placement of eCRFs.
Allows for accurate and efficient data collection.
Cons
The system does not allow a separate designation for screen failures that were lost to follow-up or who were withdrawn by the PI.
When a subject is deemed a screen-failure, eCRFs are still expected to be filled out and it is unclear which ones unless otherwise directed by the in-house team.
Return on Investment
Monitoring visits run much smoother due to the fact that eCRFs can be directly printed from the EDC.
Information requested in the EDC is clear and concise and easy to understand.