Biopharma

Your Imaging Biopartner for Pharma-Led Clinical Trials

From sponsor oversight to regulatory submission, our cloud-based imaging platform gives pharmaceutical and biotech teams full visibility and control — across every CRO, site, and study.
Request a demo
Pipeline 2-1

Trusted by Leading Pharma and Biotech Companies

logo_antaros_medical
thumbnail-scro-site-logo-dark
Boston Imaging Core lab -logo
Askel Healthcare logo green
JNJ_Logo_SingleLine_Red_CMYK
Research-Pipeline

 

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 pharma and biotech 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 Biopharma

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
More about our research solution
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
Education-Share course data-Mac Studio

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
hipaa logo
gxp gcp logo
gmp logo
iso logo
gdpr-logo
ispe gamp logo
alcoa principles logo
crf-logo

Customer cases and articles

Read more blogs

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 AWS-hosted infrastructure (ISO 27001, HIPAA, GDPR) mean your data is protected and audit-ready from day one — so you can focus on your science, not your compliance checklist.
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.