The Clinical Trials Imaging Platform
Managing trials across multiple sites often leads to inefficiencies and data inconsistencies.
Handling vast amounts of trial data demands solutions that simplify processes and ensure reliability.
Balancing multiple studies simultaneously adds pressure on Clinical Project Managers and Directors of Clinical Operations.
Collective Minds Research streamlines multi-site coordination and simplifies data management, ensuring data accuracy and trial efficiency while reducing the operational burden for clinical teams.
Seamless Multi-site Imaging Work
- Flexibility & Reliability Across the Entire Clinical Trial Lifecycle.
- Seamless, High-Quality Imaging Analysis.
- Intuitive & Easy Trial Management.
- Flexible CRF Builder for Tailored Data Collection.
- Uncompromising Data Privacy & Security.
Solutions for Contract Research Organizations (CRO)
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
Trusted by leading healthcare institutions
GDPR compliant
Leverage our GDPR compliant privacy-by-design technology to protect your patients privacy. Your data is de-identified and and pseudonymized for your collaborators while being traceable for you. Work with us, and we will support you and your hospital with the legal framework you require.





Frequently asked questions
Ready to see Collective Minds in action?
Can I set up my studies on my own?
Yes, the platform is very intuitive, and after a short onboarding, you will be able to set up your study on your own.
Can I download the data analyzed for the images?
Yes, you can create reports and share them with stakeholders depending on their role permissions.
What is the implementation process like?
Do you offer technical support or training? What kind of customer support do you provide (hours of availability, response times)?
Yes, we offer technical support and training, and the availability and response time are the same as for the regular Service level agreement. We respond on Swedish office hours.
Is there a trial period or demo available?
Can the product be customized to meet our specific needs?
Are there customizable privacy settings to control access to sensitive information?
What are the financial options available for purchasing and maintaining your platform?
Do you offer flexible pricing plans based on our usage needs and budget constraints?
Are there additional costs for scaling our usage or adding more users?
How does your platform handle collaboration among users and teams?
What level of technical support do you provide, and what are the response times?
Are there training resources or support materials available to help onboard our team?
help.cmrad.com
How frequently do you update your platform, and how do you handle feature requests?
Can we customize the platform to meet specific institutional or departmental needs?
What analytics and reporting capabilities does your platform offer?
How do you ensure the long-term reliability and sustainability of your platform?
What are the main features and how is it different from other solutions in the market? or What kind of performance benchmarks can we expect with this solution?
- Robust Compliance: Meets global regulatory requirements, streamlining audits and reducing administrative burden.
- Advanced Workflow Management: Handles complex imaging workflows with seamless integration into existing eClinical and CTMS solutions.
- Scalability: Designed to accommodate diverse study sizes and complexities, from small investigator-led trials to large-scale multicenter studies.
- Real-Time Collaboration: Enables secure, efficient communication between sites, sponsors, and CROs for enhanced decision-making and faster project timelines.
What makes us different:
- Seamless integration with eClinical platforms, reducing time-to-implementation and operational complexity.
- Superior imaging management capabilities tailored for complex trials, setting us apart from standard medical imaging tools.
- Proprietary automation features that improve accuracy and reduce manual effort.
Are there any long-term contracts, or do you offer flexible subscription models?
- Flexible Subscription Models: Tailored plans to suit your project’s duration and scale, whether short-term or long-term.
- No Long-Term Commitments Required: You can opt for month-to-month subscriptions or select plans based on the needs of your study.
- Customizable Options: For larger or ongoing projects, we also provide customized agreements to ensure the best value and support.
Feel free to contact us for more details or to discuss a plan that works best for you!
Can users from different institutions collaborate seamlessly on projects or research?
How does your platform comply with the GDPR or other laws and regulations regarding data protection and privacy?
As a dedicated Data Processor, we manage data strictly on behalf of healthcare and research institutions, ensuring it is used only for authorized research purposes and under their explicit instructions. Our platform incorporates a comprehensive framework of legal commitments, technical controls, and operational safeguards to maintain a trusted and compliant environment for data processing.
Our innovative solution, CM Connect (link), ensures that data is encrypted and pseudonymized within the institution or hospital before it is shared with our cloud. This guarantees that personal data remains protected during transfer and processing while aligning with local and EU-level privacy requirements. Once the data enters our secure cloud environment, it benefits from uniform, robust security measures that facilitate further processing in a legally compliant and ethically sound manner.
With Collective Minds, you can confidently collaborate and share data for your research projects while safeguarding patient privacy and personal data protection at every step.
What measures do you have in place to protect our data and intellectual property?
Can you provide details on where our data will be stored and how it will be secured?
AWS was chosen for its unmatched security, scalability, and global data availability, essential for a multinational clinical data sharing platform. It holds globally recognized certifications, including ISO 27001, ISO 27017, ISO 27018, SOC 1/2/3, NIS2, GDPR, and HIPAA, ensuring robust security and data protection practices.
In Frankfurt, AWS employs server replicability across multiple Availability Zones, ensuring data remains secure and accessible even in the event of server failure. The platform is also designed to meet local legal requirements worldwide (e.g., Australia, Canada, India, the US, and Europe) while maintaining consistent, stringent compliance standards across the global platform.
Our infrastructure, which includes encryption, firewalls, and continuous monitoring, ensures high availability, low latency, and fault tolerance, making it ideal for secure healthcare collaboration.

