CRITERRA operationalizes the recruitment journey through an ethical, consent-driven architecture designed to meet the rigorous expectations of Good Clinical Practice (GCP) and modern privacy standards.

Live Signal Integration
CRITERRA connects to live signals within existing healthcare systems rather than building isolated, static local databases.
Minimized Footprint
By utilizing a real-time provider integration mesh, we reduce the risks associated with data redundancy and outdated patient lists.
Explicit Consent
Patient referrals are only initiated after explicit consent is captured at the healthcare touchpoint.
Transparent Routing
Candidates are routed directly to authorized research sites through secure, documented workflows.
Full-Funnel Documentation
We provide measurable visibility from the initial match through to enrollment, ensuring every referral is traceable.
GCP Alignment
Our reporting is designed to support regulated clinical environments and audit-friendly oversight for Sponsors and CROs.

CRITERRA is built on over two decades of clinical research leadership across Phase I–IV trials, including global pharma and oncology operations. We understand the nuances of site execution and sponsor requirements intimately.
We maintain detailed documentation for privacy and security reviews by participating healthcare organizations and CROs. Specifics regarding our pilot deployments and technical integrations are available for review under NDA.
Request Security Documentation