Audit-ready by default. carGO Health provides clinical trial specimen transport and investigational product delivery with the documentation that satisfies FDA, ICH-GCP, and sponsor SOP requirements. Temperature-documented, HIPAA-compliant, chain-of-custody tracked from site to lab. Trusted by Episteme Prognostics for precision medicine research. Our medical courier service was built for this level of accountability.
In clinical trials, a specimen without proper documentation is a specimen that doesn’t exist. FDA inspectors, sponsor auditors, and IRB reviewers expect to see documented proof that every specimen was collected, transported, and delivered under protocol. Temperature excursions, chain-of-custody gaps, and missing timestamps don’t just create compliance risk—they can invalidate trial data.
carGO Health provides digital chain-of-custody, continuous temperature logging, CLIA/CAP compliant documentation, and real-time tracking that gives your clinical operations team the records they need—before the auditor asks for them. OSHA-compliant couriers with proof of delivery for every handoff.
CROs & Sponsors: Multi-site specimen collection with unified documentation across all trial sites.
Research Institutions: University-based clinical trials with specimens requiring refrigerated, frozen, or cryogenic transport.
Biotech & Pharma: Investigational product distribution and biologics cold chain logistics.
Hospitals: Hospital-based trial sites needing STAT and scheduled routes specimen pickup.
carGO Health covers the full Northeast: New York (all 5 boroughs, Long Island, Westchester, Hudson Valley, Upstate), New Jersey, Connecticut, Massachusetts, Pennsylvania, Delaware, Maryland, Virginia, New Hampshire, and Vermont. Learn more about our comprehensive medical courier service.
Yes. Digital chain-of-custody, temperature logs, timestamps, GPS records, and courier certifications—all audit-ready and exportable.
Yes. Unified documentation across all sites. Multi-site logistics coordination.