Medical Storage: GDPR and MyHealth@EU compliant platform for clinical trial and medical research data
A global healthcare company had fragmented tools for managing its global clinical trial and research data. CML Team built a secure, centralized platform for managing clinical trial and medical research data. The solution improved data accessibility, compliance and operational efficiency. It reduced trial setup time.
- Client country
- Switzerland
- What we did
- Built the fault-tolerant, microservices-based backend system; the work covered technical decision-making, scaling the platform to a cloud enterprise solution and code quality improvement.
Who is the client behind Medical Storage?
A global healthcare corporation ($250B+ market cap) operating across pharmaceuticals, medical devices and clinical research. It collaborates with hospitals and research institutions worldwide to lead innovation in large-scale clinical trials.
What problem did Medical Storage have?
The client lacked a centralized, secure and compliant system for managing global clinical trial and research data. Existing tools were fragmented, limiting collaboration, standardization and integration. It needed a scalable solution with strict data protection (MyHealth@EU), strong access control and high availability.
What did CML Team build for Medical Storage?
- Secure, centralized platform for managing clinical trial and medical research data
- Fault-tolerant, microservices-based backend system for centralized data management
- Scalable microservices architecture
- Planning, execution and standardized structuring of clinical trial data
- Granular access control
- GDPR and MyHealth@EU compliance
- Compliance with EU medical data standards
- 99.9% uptime
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- Smooth integration with 10+ external services
- 80%+ test coverage across the infrastructure
- Scaling of the platform to a cloud enterprise solution
- Code quality improvement
What was the result for Medical Storage?
The system streamlines clinical trial planning, data structuring and sharing between research teams and external partners. Integrated with 10+ external services, it supports high data security, reliability and operational efficiency. The solution improved data accessibility, compliance and operational efficiency. It reduced trial setup time, enabled secure global collaboration and provided a scalable foundation for future research initiatives. The client now operates on a strong, regulation-ready platform for accelerating medical innovation.
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