The problem we solve
Many synthetic data providers create their datasets manually, which takes much longer to do, with severe implications for the complexity, reliability and availability of the data they are able to offer. TrialTwin™ brings you fresh synthetic data as often and as fast as you need it.
Not manually created
Many synthetic data providers create their datasets manually, which takes much longer to do, with severe implications for the complexity, reliability and availability of the data they are able to offer. TrialTwin™ brings you fresh synthetic data as often and as fast as you need it.
Not taken from real patients
Unlike real-world data from real-life patients, TrialTwin™ synthetic health data comes with no privacy or security constraints, no copyright costs, and no need for any special safeguarding measures.
Faster study start-up
The TrialTwin™ platform speeds up the process of getting new clinical trials from the planning phase to FPI, and onwards to successful completion, shortening the cycle of approval of new drugs and medical devices.
Increase the rate of successful completion
Most clinical trials do not reach successful completion, a common cause of failure being lack of the sufficient ability to plan. TrialTwin™ enables thorough and sophisticated testing of systems and processes before a trial is even registered, at high speed and low cost.
Plan studies faster and more thoroughly
Use TrialTwin™ to experiment with and test ideas you may have for future trials, before you reach the stage of setting up and registering a study, or enroll patients. Use TrialTwin™ again at each stage when changes are needed during a trial.
Visit the available free samples
created for active clinical trials
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A DEMO
Our in-house team will be delighted to give you an in-depth view of the power and capabilities of the TrialTwin platform.