Take control of imaging across your clinical trials

Centralize imaging operations, strengthen CRO and site oversight, and ensure submission-ready data, all from a centralized cloud-based imaging platform built for sponsors.

Talk to a specialist

Explore the platform

Trusted by Leading Pharma and Biotech Companies

Sponsoring trials across multiple CROs creates blind spots — inconsistent data, fragmented workflows, and limited real-time visibility

Regulatory submissions demand complete, audit-ready imaging data — manual processes put timelines and compliance at risk

Scaling from Phase I to Phase IV requires systems that grow with your study, not ones that break under complexity

Collective Minds Research gives sponsors a single, compliant platform to design trials, oversee CRO operations, manage imaging data, and prepare submission-ready packages — all in one place

Clinical trials with imaging endpoints shouldn’t slow you down

Full Sponsor visibility across all sites and CROs
Submission-ready audit trails (21 CFR Part 11)
Customizable eCRFs aligned to your study protocol.
Role-base access for sponsors, Cros, and sites.

Clinical-Grade DICOM viewer.
Automated DICOM unonimyzation.
Seamless Integration with eClinical and CTMS systems.
Scalable from Phase I to phase IV

Solutions for Sponsors

Research

Run your clinical trial with ease using Collective Minds Research.

Intuitive Interface
Seamless Integration
Efficient Data Sharing
Scalability and Flexibility
Data Security and Confidentiality

Design your trial with precision

Lightning-fast data collection

Unmatched expert and site network

Decades of proven expertise

Clinical-Grade DICOM viewer

An integrated clinical grade DICOM viewer ensures that educators and learners have access to professional high quality imaging tools: presenter and measurement tools, PET-CT, Mr and NM Fusion, Histogram, Calibration line, MPR, CINE, Align and lock, sync Windowing and many more.

Education-DICOM Viewer-Galaxy Tab S8 Ultra

Share data for your course quicker and easier

Connect your hospital or local computer using CM Connect. This way you can share any DICOM studies automatically. Before the data is transferred from your local environment, it is de-identified and pseudonymized. This allows your preparation to be focus/topic driven.

1 200+

Researchers

300+

Connected Sites

300+

Imaging Trials Running

Frequently asked questions

Everything you need to know about using Collective Minds for clinical trials, research, and collaboration.

More questions? More answers!

We’ve got a big collection of answers.

Visist FAQ page

Does Collective Minds Research meet the regulatory standards required for clinical trial submissions?

Yes — and it's built so your team doesn't have to think twice about it. The platform is fully compliant with 21 CFR Part 11, generates complete electronic audit trails, and produces submission-ready imaging packages out of the box. Automatic DICOM de-identification, validated workflows, and secure infrastructure mean your data is protected and audit-ready from day one — so you can focus on your science, not your compliance checklist. Collective Minds operates an Information Security Management System certified to ISO/IEC 27001:2022 by A-LIGN. Our platform is hosted on AWS, whose infrastructure holds ISO 27001, ISO 27017, ISO 27018 and SOC 1/2/3 attestations.

We work with multiple CROs across different geographies. Can Collective Minds handle that complexity?

That's exactly what it's designed for. Collective Minds Research gives sponsors full visibility across every CRO, site, and study — all from a single platform. Role-based access ensures each party sees only what they should, while you maintain centralized control over data quality and timelines. No more chasing CROs for status updates or reconciling fragmented datasets. Everything is in one place, in real time.

We're currently in Phase I — is it too early to implement Collective Minds Research?

Not at all — in fact, it's the ideal time. Starting with Collective Minds from Phase I means your imaging infrastructure, data standards, and audit trails are already in place when you scale to Phase II, III, and beyond. You won't need to migrate data, retrain teams, or rebuild workflows mid-trial. The platform grows with your study, so the earlier you start, the more value you get.

Insights

Imaging Trial Solution Collective Minds Research

See it in action

Book a demo and see how you can securely share medical imaging data, collaborate across institutions, streamline research and clinical workflows.

Book a demo