Delve Health

Biotechnology ResearchMinnesota, United States11-50 Employees

Clinical trials weren’t built for people. So we built something better.

At Delve Health, we help biotech, medtech, and biopharma teams run smarter, faster clinical trials, with Quality by Design (QbD) and ICH E6(R3) compliance at the core.

We’ve rethought the way trials should run, replacing fragmented vendor stacks and bloated CRO workflows with one purpose-built platform. From protocol design to final submission, Delve helps teams reduce risk, increase compliance, and accelerate results.

What makes us different:
✅ QbD-first, ICH-aligned. Workflows are protocol-driven from Day 1, not added later. Every form, alert, and reminder is tied to your endpoints.
✅ Direct data capture. Device + patient data flows directly into your study — no transcription, no middleware.
✅ Risk visibility in real time. Our platform flags compliance gaps, missing data, and at-risk patients automatically, before it becomes a problem.
✅ Virtual coordinators. Our patient-facing team reduces site burden and keeps participants engaged.
✅ API-first architecture. We plug into your stack; EDCs, labs, eConsent, and beyond.
✅ Multilingual + global-ready. 100+ languages, BYOD or provisioned devices, and concierge-powered retention.

We’ve helped sponsors cut study costs by up to 35%, improve compliance to 90%+, and reduce site workload, all while staying aligned with the latest ICH and GCP guidance.

If your trial still depends on 5 vendors, spreadsheets, and Friday site calls — let’s talk.

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