The Power of Ten Systems
The Simplicity of One makes clinical trials seamless by bringing together the best and most important functionality of Study Design & Protocol Optimization, Trial Administration, Data Collection & Task Management all in one intelligent system. We provide compliant roles-based logins for

Trial Sponsors, Sites, Study Subjects, Monitors & Consultants

Choose only the functionality you need and nothing you don’t.

AI for Study Design Optimization’s Study Optimizer provides insights using massive amounts of data from past clinical trials, medical journals, and real-world sources to identify risk factors and provide recommendations for optimizing your trial.

1. Upload your protocol  

Submit your initial protocol to be analyzed.

2. Identify risk factors looks for risk factors that could lead to things like future amendments and difficulties in recruitment and retention.

3. Get recommendations provides recommendations to optimize your protocol.


Our NLP Platform

Our AI platform helps you to optimize your study designs by mining massive amounts of related source documents so that you don’t have to – all with an intelligence that comes with our targeted training/tuning with healthcare and specifically trials domain data. We have a fully developed pipeline of NLP processors that provide Native support for Microsoft Word & PDFs.

Simple Workflow Reduces Errors

  • Improve adherence using machine learning to analyze, interpret and respond to user behavior.

  • Intelligent assistance navigates stakeholders through trial and minimizes subject dropout.

  • Dynamic process monitoring to boost efficiency for sites and minimize subject burden. 



Real-Time Insights for Sponsors

Course correct based on real-time actionable data on enrollment, retention, adverse events, adherence and more.

Immediate feedback on underperforming sites for trial rescue.

Daily alerts for threats to timelines.

End-to-end planning and execution tools.

Better Protocol Adherence is protocol driven, meaning it intelligently guides researchers and participants through the protocol events. It enables everyone to spend less time being burdened with administrative tasks and keeping track of “to-do’s” and more time on the things that ensure trial success, like clean data collection.

An Extra Project Manager is your study coordinator’s best friend. It helps manage monotonous day-to-day activities like intelligently computing patient eligibility, managing patient visits, remembering important protocol information, and keeping track of what events need to be done, so they can focus on what really matters: caring for participants.

Find out how to get started TODAY!

Easy Interactions for Patients

Making it easy for participants to enroll and engage in clinical trials is a top first priority for us. That’s why we designed a digital experience for them that is incredibly simple and intuitive and can be accessed through any web-enabled device. takes the burden off of participants by guiding them through the entire trial, letting them know what they need to do, and when. By making it simpler for participants to enter data, schedule appointments, and access important documents, we help organizations conduct cleaner, more efficient trials.

After all, when we make the process better for participants, we make it better for everyone.