Global imaging CRO services

We have reimagined what it means to be an imaging CRO. We deliver our services using a modern, high-performance imaging platform designed for speed, scalability, and reliability. Embedded workflow tools improve image handling in clinical trials, accelerating patient inclusion through a proprietary infrastructure to rapidly onboard sites and evaluate patients in days, not weeks. We provide a complete end-to-end service and do not outsource to third-party vendors.

Global imaging CRO services
“At Qureight, we didn’t just build an imaging CRO—we reimagined it from the ground up. Every tool, every workflow, every process was designed to tackle the real pain points of clinical trials: the delays, the inefficiencies, and the frustration of unusable data. We’ve turned slow study start-ups into rapid launches, complex site initiations into seamless onboarding, and poor data quality into precision insights. Welcome to the new standard for clinical trials.”

Dr Steven Bishop

Chief Medical Officer

Key advantages of our CRO services

1. Efficient and effective study management

Our services are designed for efficient study start-up, including a cloud-hosted, globally available platform and automated validation for improved adherence to the Imaging Charter.

2. Site centric / friendly

Our tiered remote site qualification process is built for fast site activation and protection of First Patient In (FPI) timelines. We support a wide range of real-world CT scanners and protocols. There is no need for complex or time-consuming image acquisition, phantom scans or respiratory gating.

3. Fast, accurate central read turnaround

We provide expert central reader teams comprising named radiology key opinion leaders with extensive clinical trial experience to improve consistency. Our read forms are co-designed by our experts to help you maximise utility and consistency. We guarantee a 72-hour turnaround time for all eligibility reads.

4. Integrated AI insights and endpoints

Qureight's AI-powered endpoints and analytics are integrated into our platform. These support cohort enrichment strategies and automated reporting of disease severity across all enrolled patients.

5. Built for compliance

The Qureight platform provides secure image transfer, global data privacy compliance, built-in quality controls and full auditability. It’s compliant with GCP, GAMP 4/5, EMA CSV, 21 CFR Part 11, ISO 27001, ISO 13485, GDPR, and HIPAA.

6. Backed by world-leading expertise

We provide access to globally recognised key opinion leaders in lung and heart disease, including in-house expertise, our disease-specific Scientific Advisory Boards and advisor KOLs.

  • Avalyn Pharma’s preferred imaging partner

    Avalyn Pharma’s preferred imaging partner

    When Avalyn sought an imaging partner capable of delivering scientific excellence and AI-powered biomarkers, they turned to Qureight in 2024. Recognising our ability to address the industry’s most pressing challenges – slow study start-ups, cumbersome site initiations, inconsistent data quality, and precision analytics – Avalyn made Qureight its preferred imaging partner in 2025. Today, we power imaging operations for their MIST, AURA, and SAIL studies, leveraging our high-performance platform to accelerate patient inclusion, ensure flawless data quality, and deliver our quantitative imaging biomarkers at scale.

  • Accelerated trial start-up timeline

    Accelerated trial start-up timeline

    When Rein Therapeutics, Inc faced study start-up delays Qureight was able to step in as their imaging partner to deliver on time results. With an ambitious four week timeline for study start-up, we leveraged our proprietary platform and streamlined workflows to rapidly onboard sites, optimise image handling, and ensure seamless data integration. Qureight proved that speed and precision can go hand in hand. For Rein, this meant no compromises: accelerated timelines, flawless execution, and a partnership built on reliability and results.

Find out how we can
suport your clinical trial