Smarter Observation for Clinical Research
Structured tools for site visits, remote monitoring, and protocol compliance observation — built for CRAs, sponsors, and research coordinators.
Site Monitoring & Audit Tools
Standardized observation checklists for site initiation, routine monitoring, and close-out visits. Capture findings, flag deviations, and generate visit reports in a consistent format that satisfies sponsor and regulatory expectations.
Remote Monitoring Workflows
For decentralized and hybrid trials, Spy Clinic supports remote source data verification, eISF review workflows, and asynchronous query management. Designed to reduce travel burden without reducing oversight quality.
Frequently asked questions
- Is Spy Clinic validated for use in regulated trials?
- We offer a 21 CFR Part 11-aligned configuration. Full validation documentation is available on request.
- Can it integrate with existing EDC systems?
- API integrations with major EDC platforms are available on our enterprise plan.
- Who is the typical user?
- Clinical Research Associates, study coordinators, and sponsor oversight teams at biotech, pharma, and CROs.
Get in touch
CROs, sponsors, and site teams — contact us for a demo or to discuss enterprise licensing and validation support.
research@spy.clinic