The Integration Layer for
Life Sciences
Running a modern trial means moving data between EDC systems, eCOA patient devices, lab information systems, imaging platforms, wearables, and electronic Trial Master Files. The vendor landscape is dominated by proprietary ecosystems that don't integrate well with each other, so teams fall back on manual data reconciliation that adds cost and introduces errors.
The Clinical Trial Integration Problem
Running a modern trial means stitching together a fragmented vendor ecosystem under some of the strictest regulatory requirements in any industry.
Proprietary Silos
The major EDC, CTMS and eTMF platforms lock data into proprietary ecosystems. Running a best-of-breed stack means building custom integrations between every pair of systems: EDC to CTMS, CTMS to safety, safety to regulatory.
Regulatory Complexity
FDA 21 CFR Part 11, GxP validation, ICH-GCP guidelines, and EU Clinical Trials Regulation impose strict requirements on data integrity, audit trails, and electronic records. Generic automation tools cannot meet these standards.
Multiplying Data Sources
Decentralised trials add wearables, remote monitoring, and telemedicine data streams that must flow into trial databases with full traceability. Each new data source is another integration to build and validate.
Life sciences are on our roadmap.
iGaming is live today. Tell us about your life sciences integration needs and we will be in touch.