Solutions for Contract Research Organizations
CliniQR helps CROs streamline patient recruitment and retention across multi‑site trials using secure, QR‑based consent and real‑time patient engagement—without storing PHI.
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Designed to fit seamlessly into CRO‑led trials—without disrupting site workflows.
Reduce time‑to‑screen by enabling patient‑friendly, QR‑based outreach, pre‑screening, and consent—online or on‑site.
Wrap around existing site systems and workflows. No new platforms for coordinators to learn. No process replacement required.
Tokenized events, encrypted messaging, and no PHI storage help minimize audit exposure while supporting HIPAA and 21 CFR Part 11.
A standardized patient journey that works across sponsors, sites, and regions.
QR‑enabled campaigns and referrals
Eligibility questions and consent capture
Labs, imaging, diagnostics
Automated reminders and coordination
Eligibility confirmed, trial entry
Long‑term retention and outcomes
CliniQR integrates into existing clinical trial environments without requiring CROs or sites to replace their EHR, CTMS, or operational tools.
CliniQR supports CRO compliance obligations through secure design, audit‑ready workflows, and patient‑centric consent handling.
PHI minimization and encryption
Electronic records & signatures support
Secure patient authentication
Immutable event‑based consent
See how CliniQR supports faster enrollment, stronger retention, and lower operational risk across your trial portfolio.
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