
For Medtech and Biotech companies running regulatory imaging clinical trials, who need to accelerate trial timelines while ensuring strict compliance.
Collective Minds is a clinical trial automation platform that streamlines complex processes, guarantees full GCP compliance, and speeds your path to market.
Unlike traditional manual approaches, it transforms trial design into controlled workflows, enables instant imaging data collection and de-identification, and provides access to the largest expert and site network backed by decades of proven experience.
- Managing an imaging trial shouldn’t be this complicated. Yet too often it is. Ad-hoc reviews, manual data transfers, and fragmented workflows create unnecessary cost and delay. The result? Slower studies, weaker data, longer path to market and even risk of failure.
- Collective Minds provides a central platform to implement, execute, and manage your entire imaging trial. The platform is easy to use and requires no installation, while features like automatic data transfer, image de-identification, and central image review ensure GCP compliance.
- Combining powerful automation with our team of top imaging experts and an established network of clinical sites, making your trial successful, fast, and affordable.


How?
- Design Your Trial with Precision: We turn your imaging trial design into an automated workflow where every step is a controlled event. This ensures each task—from data collection to a blinded central independent review (BICR)—is executed with precision and assigned to the right person, every time.
- Lightning-Fast Data Collection: Our platform automatically collects and de-identifies imaging data, getting it from the trial site to project review in minutes. This eliminates slow traditional methods and keeps your trial moving at top speed.
- Unmatched Expert and Site Network: Gain instant access to the industry's largest network of clinical professionals, with over 30,000 imaging experts and more than 300 imaging sites across Europe and the U.S.
- Decades of Proven Expertise: Our team brings hundreds of years of combined experience in designing imaging technology, developing biomarkers, and managing complex clinical trials. When you work with us, you're working with the best in the industry.
Benefits and Features
- Implement your imaging trial design as a "string of controlled events", using the pipeline. Each event is associated to project roles, automation and notification. E.g. blinded central independent review (BICR) with clinical adjudication.
- Automated data collection and de-identification of image data, from sites to project QC in less than 10 minutes with Connect.
- Access the largest network of clinical experts (+30.000 imaging experts) and imaging sites (+300 in Europe and the US).
- Work with the best imaging team in the industry. Hundreds of years of experience in designing imaging technology, biomarkers and managing clinical trials.

Solutions for MedTech and BioTech
Research
- Intuitive Interface
- Seamless Integration
- Efficient Data Sharing
- Scalability and Flexibility
- Data Security and Confidentiality
Connect
Automate your imaging data transfers from modality to results.
- Automatic end to end data flow.
- Seamless PACS Integration
- Advanced Pseudonymization
- Secure Reliable Transfers
- Multi channel support
Trusted by many customers and three of the biggest pharmas







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
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?
We will support you throughout the entire implementation and deployment process. A Customer Success Product Specialist will assist you with any questions you may have during onboarding activities. From user training and onboarding to creating Standard Operating Procedures (SOPs) and conducting compliance audits, our team will provide comprehensive support.
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?
Yes, we can provide you with a trial period to explore the basic capabilities of the platform, allowing you to evaluate if this is the right choice for you.
Can the product be customized to meet our specific needs?
The Collective Minds Research Platform is highly customizable to meet your needs, whether you're conducting a Phase III clinical trial or a reader study. You can configure the project pipelines to precisely match your study design, and easily add new members and sites as needed. Additionally, our integration capabilities allow you to connect Collective Minds Research with your existing systems, ensuring maximum flexibility and efficiency.
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?
The pricing follows the agreed-upon price plan from initial signatures. If usage exceeds the initial agreement, pricing may increase based on our pricing table's tiers.
How does your platform handle collaboration among users and teams?
You can configure roles and permissions for each project member, which allows you to grant access to shared tasks and make results visible to all team members. To invite someone to a project, simply enter their email address and name.
What level of technical support do you provide, and what are the response times?
The Customer Success team will support you with project configurations and platform features, customized to align with your specific agreement. Our office hours are Monday through Friday, from 9 AM to 5 PM. Depending on your needs, we can provide SLA-based support as well.
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?
Our platform undergoes regular updates, including major feature releases several times a year and ongoing critical patches and security enhancements. We prioritize feature requests based on a structured process that considers client feedback, market trends, and technical feasibility. Feature requests are evaluated based on their potential impact and alignment with our roadmap. We keep clients informed about major updates and new features through our release announcements and newsletters.
Can we customize the platform to meet specific institutional or departmental needs?
What analytics and reporting capabilities does your platform offer?
The results will be exported in .csv format, making it easy to import them into any statistical analysis software that supports this format, such as Excel. The results can aslo be stored as uneditable reports, where delivery is managed and logged through the platform. As of today, the platform does not offer built-in analytics tools.
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?
The main features of our solution are: - Automated De-identification and anonymization: Ensures patient privacy and compliance with strict regulatory standards.
- 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?
Collective Minds research is designed with collaboration in mind. In a research project, you will have the opportunity to define the roles and site affiliations, no matter which institution the members belong to.
How does your platform comply with the GDPR or other laws and regulations regarding data protection and privacy?
Collective Minds is designed to empower healthcare and research institutions by providing a secure and compliant platform for data sharing. We address the critical challenges of safeguarding patient privacy and ensuring data protection while enabling collaboration. Rooted in privacy by design, our platform offers a secure processing environment that adheres to the highest privacy standards, including the General Data Protection Regulation (GDPR).
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.