Integrated DICOM Imaging, Core Lab Workflow, and AI-Powered Compliance
When imaging works seamlessly, everything moves faster
In your clinical trial, imaging is not just another data stream.
It drives patient eligibility, informs safety assessments, and defines critical clinical endpoints.
You rely on clinical trial imaging data to make decisions quickly and with confidence.
Catchtrial Medical Imaging is designed to support exactly that—delivering a fully integrated imaging workflow where DICOM data capture, Core Lab review, and compliance processes fit naturally into your trial, without slowing it down.
Everything connected, from the start
When imaging works seamlessly, everything moves faster
With Catchtrial, your clinical imaging workflow is not managed in a separate system.
It is built directly into your EDC (Electronic Data Capture system).
This means that when sites upload DICOM images, they are instantly aligned with your protocol, patient visits, and study structure. There is no need for reconciliation, no duplicate tracking, and no disconnected platforms.
Your clinical imaging data and trial data are unified from the beginning, ensuring consistency, traceability, and efficiency across your study.
From DICOM upload to Core Lab review—without interruption
Sites can upload DICOM images directly within the eCRF, using a secure, web-based interface.
From there, the process is fully automated. Images are prepared, anonymized, and transferred securely to your Core Lab imaging environment, where they are available almost immediately through a high-speed streaming DICOM viewer.
Your teams do not wait for downloads or manual transfers.
They can start reviewing images in real time.
This enables faster eligibility assessment, endpoint adjudication, and clinical decision-making.
AI-powered anonymization and compliance—built in
Handling medical imaging data in clinical trials requires strict compliance with global regulations.
Catchtrial uses AI-driven technology to remove protected health information from both DICOM metadata and burned-in pixel data, ensuring full alignment with HIPAA and GDPR requirements.
This advanced DICOM anonymization approach reduces site burden while maintaining the highest standards of data protection.
At the same time, every action is recorded, providing a complete audit trail and ensuring inspection-ready clinical trial data.
A Core Lab imaging platform designed around your study
Your Core Lab should focus on analysis—not coordination.
Catchtrial provides a fully integrated Core Lab management platform, where imaging data, adjudication forms, alerts, and reports are all connected within a single, study-specific environment.
Your team has real-time visibility into image status, completeness, and quality. This allows for efficient centralized imaging review and endpoint adjudication, without the need to manage multiple systems.

Faster decisions, cleaner data, stronger trials
When your imaging workflow is fully integrated, your trial moves forward with clarity.
Screening becomes more efficient because imaging data is available immediately.
Adjudication progresses continuously rather than being delayed.
Data remains structured, consistent, and traceable from day one.
This supports faster clinical trial execution, improved data quality, and smoother regulatory submission.
Proven for global clinical trials and high-volume imaging
Catchtrial Medical Imaging is already supporting global, multi-center clinical trials, particularly in cardiovascular and imaging-intensive therapeutic areas.
The platform is designed to handle large-scale DICOM imaging datasets, connect sites and Core Labs worldwide, and support high-performance clinical trial operations.
Clinical imaging that works the way you need it to
You are running a complex clinical trial with high expectations.
Your imaging platform should support that—without adding operational burden.
Catchtrial Medical Imaging delivers a connected, scalable, and compliant clinical imaging solution, enabling you to manage DICOM data, streamline Core Lab workflows, and generate approval-ready evidence with confidence.

