Compliant, Scalable, and Built for Patient-Centric Research
Capture, manage and validate clinical trial data in real-time.
Empower patients to report outcomes from any device, anywhere.
Randomization and supply management tailored to your protocol.
Digitally engage participants and streamline informed consent.
Direct Data Capture from sites with real-time verification and automation.
Automate adverse event and medication coding using industry dictionaries.
Targeted Workflows for adaptive study needs and cross-functional collaboration.
“Built and deployed EDC for a 10-country Phase III heart failure trial in under 6 weeks.”
— Clinical Project Manager, Global CRO
Let’s talk about how our technology can accelerate your research.
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