Our Product

How it Works

By integrating AI and machine learning, the Comonitor software will be able to take most site provided source and extract key data points to then verify against the inputted EDC data. Why is this important? Through the use of automation Comonitor can drastically reduce your clinical trial SDV expenditures and clinical trial data timelines.

Advantages Vs Traditional CRA SDV Monitoring

• Traditional CRA SDV monitoring is labor and time intensive.
  • Comonitor can function 24/7 and is programmed with efficiency in mind.
• CRAs are limited by time and fatigue in their ability to SDV. The industry standard of 60 pages per 8-hours is a testament to that.
  • Comonitor can complete an entire clinical trial, if source is given, in less than 30 minutes
• Through the use of Comonitor, CRAs will have more support and time to focus on Data Review.

These are only some of the benefits Comonitor can provide you. Reach out to us via email to learn more!