Today, most startups outsource their clinical studies to contract research organizations (CROs), paying high costs for slow, manual, and error-prone processes. We take the opposite approach: empowering lean teams to run trials themselves with tools that are faster, simpler, and compliant from day one.

Our first product is a fully GCP and 21 CFR Part 11-compliant electronic data capture (EDC) system that with AI-assisted study builds; automated source data entry; and real-time remote monitoring. The result: higher-quality data, faster timelines, and dramatically lower costs without compromising on security and compliance.

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