PRODUCE YOUR STATISTICAL
REPORT 10X FASTER
Our mission is to revolutionize the way you will run your next clinical trial.
We know that study success is a company responsibility. By integrating data collection and data monitoring across all the touchpoints of your study, we help you eliminate non-value-added people and paper, accelerate your time to results and maximize your study success.
We do all of this in a secure cloud at unprecedented price points - 30-50% cheaper than any competing paper or cloud EDC/Risk-based-monitoring solution on the market today.
For medical device and biotech startups
Produce your statistical report up to 10X faster by eliminating the rework typical in paper CRF. Use our Risk Apps to stay on top of your sites, your subjects and your CRO.
Use our Risk Apps to hit your milestones with actionable intelligence on sites. Be more effective with 5-10X better ROI on your monitoring dollar.
Your early-stage startups as well as your later stage portfolio companies accelerate product development with the most cost-effective tools on the market today.
Access all the data, anytime, from anywhere.
Risk Apps identify safety, data quality and protocol compliance issues without expensive and limited-value on-site monitoring visits.
No need for IT. Just use it.
Bespoke tailoring for your trial to get the insights you need to succeed.
Clear Clinica is 30-50% cheaper than any competing product.
Best practices for implementing EDC Systems in clinical trials
Having a well-planned and executed implementation of the Electronic Data Capture system for your clinical trial is crucial to succeed with it.
- Learn the 6 step program to EDC success
- Correct EDC misconceptions/dispelling the FUD
- Find out the best practices for the implementation of EDC