CLINICAL TRIAL IMAGE MANAGEMENT
To support imaging-driven clinical trials, Veron works with leading experts in clinical imaging
Veron Scientific provides independent expertise in clinical trial imaging and image management. We support sponsors, biotech and CROs in establishing efficient and compliant imaging workflows aligned with study objectives through close collaboration with specialised imaging experts.
The imaging team supporting these activities brings more than 25 years of international experience in medical imaging and clinical trial image management.
- Imaging Project Management
- Clinical Trial Image management
- Imaging Biomarker Consultancy
- CTIMS (Clinical Trial Image Management System) Support
- Image Quality Control & Processing
- Imaging Documentation & Charter Support
- Vendor & Technology Selection
- Site & Study Team Training
- EDC Data Entry & Verification
- Central Reader Management
Imaging Project Management
Practical oversight and coordination of imaging activities throughout the study lifecycle, ensuring timelines, milestones and deliverables are met. This can include participation of an imaging dedicated senior Imaging Project Manager in trial project meetings.
Clinical Trial Image management
End-to-end management of imaging workflows—from site setup and image acquisition to secure transfer, tracking, quality control and final delivery. Includes imaging platform selection (EU- or US based) and batch image (re)anonymisation.
Imaging Biomarker Consultancy
Expert support in defining imaging endpoints, developing image read strategies, and integrating imaging biomarkers into clinical trial protocols.
CTIMS (Clinical Trial Image Management System) Support
Guidance on the development, optimisation and implementation of Clinical Trial Image Management Systems tailored to the operational needs of each study. Services can include or solely be user acceptance testing or pre-live testing to determine if a system is well tailored to match trial set-up
Image Quality Control & Processing
Independent image quality review and structured image processing to ensure consistency, protocol compliance and data integrity across all participating sites.
Imaging Documentation & Charter Support
Preparation and review of imaging charters, SOPs and study documentation to ensure operational clarity and alignment with regulatory expectations. Preparation of Imaging guidelines/protocols, Imaging Charters (IRC), SOPs and other relevant documentation to ensure operational clarity, Imaging consistency for various sites.
All documentation focused to serve the study’s imaging endpoints and in alignment with regulatory expectations.
MRI Various Techniques and MRI Sequences
CT Diagnostic Guided Biopsy CT-Angiography
X-Ray Regular & Advanced Clinical Views Mammography
Vendor & Technology Selection
Support in evaluating and selecting imaging core laboratories, AI technology providers, image transfer solutions and specialised medical imaging software.
Site & Study Team Training
Targeted training for investigational sites, CRAs and sponsor teams to support imaging compliance, protocol adherence and operational consistency.
EDC Data Entry & Verification
Accurate entry and verification of imaging related data within EDC systems to maintain traceability, quality and audit readiness.
Central Reader Management
Coordination and oversight of central imaging readers to ensure consistent image assessment, adherence to read charters and timely reporting of results.
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