Control, visibility, and inspection-ready imaging data
SliceVault is a cloud-based software platform for securely transferring and managing medical images in clinical trials, from site submission and automated de-identification through structured QC and central review.​
​Role-based, audit-ready controls give sponsors real-time oversight without the cost and complexity of enterprise suites.
Core clinical trial imaging capabilities
SliceVault streamlines secure image submission, automatic de-identification, structured quality control, and central review — all tracked with audit-ready controls.
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As a cloud platform, SliceVault provides global, browser-based access without software installation or infrastructure overhead.
Five reasons sponsors choose SliceVault
Clinical trial imaging is complex, fragmented, and tightly regulated. Imaging data is generated at many sites, handled by multiple partners, and reviewed over long timelines. Yet sponsors remain accountable for data integrity, inspection readiness, and operational risk — often without real-time visibility into submissions, quality control, reading workflows, or progress.
01
Real-time oversight that keeps you in control
Sponsors need ongoing visibility into imaging data quality, submission status, and read progress. SliceVault centralizes these insights in one cloud system, so you can identify issues early, understand study trends, and act with confidence — without micromanaging execution or relying on fragmented reports from partners.
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This helps reduce operational risk throughout the study lifecycle.
What sponsors say
The most outstanding function for our clinical trial is the simple but effective overview of all the visits of our study subject in one clear interface. Furthermore, the colour coding of the visits is very useful when it comes to keeping an overview of what has to be done with every visit...
Jim Bakker | Clinical Associate | Amber Implants
02
Controlled governance without disruption
SliceVault is a standalone cloud software that provides a controlled environment for clinical trial imaging, operating alongside your existing clinical technology landscape.
Through role-based access and study-specific workflows, you define who sees what and when, keeping accountability clear across sponsors, CROs, core labs, and sites.
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This preserves structure while supporting multi-party execution.
03
Protocol-aligned workflows that adapt without risk
Clinical trials rarely follow a single template. SliceVault workflows can be configured to match study protocols across submission, QC, and reading
We continuously evolve the platform based on customer needs and study learnings, and when changes are necessary we adapt in a controlled, documented way that preserves oversight, traceability, and compliance.
04
Purpose-built imaging, without unnecessary cost
Enterprise clinical suites often bundle imaging into broad, expensive platforms you don’t fully use. SliceVault’s purpose-built imaging platform lets you pay for what you actually need, start studies faster, and avoid overhead from unused modules — all without sacrificing the controls sponsors require.
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This keeps imaging spend aligned with study needs and reduces operational overhead.
Area
SliceVault
Enterprise platforms
Platform scope
Purpose-built for imaging
Imaging bundled into large clinical suites
Cost model
Aligned to study scope and duration
Long-term, multi-module licenses
Implementation
Fast study startup
Long onboarding and configuration
Flexibility
Configurable, with optional bespoke extensions
Rigid, standardized workflows
Sponsor oversight
Direct, real-time visibility
Often abstracted behind CRO layers
Imaging focus
Dedicated imaging workflows
Imaging as a secondary module
05
Compliance at the forefront
SliceVault is fully validated, regularly audited, and designed to support regulated imaging workflows, including 21 CFR Part 11, GDPR and HIPAA. Complete audit trails, role-based access, and controlled processes help sponsors maintain inspection readiness throughout the study. We welcome vendor assessments and provide relevant quality and validation documentation to support your review.
