Charité VRE Secure Processing Environment
Service Description
Overview
The Charité Virtual Research Environment (VRE) provides a Secure Processing Environment (SPE) and Trusted Research Environment (TRE) for collaborative processing, exchange, and analysis of human health data in the context of GDPR, AI Act compliance, MDR evidence generation, and Post-Market Clinical Follow-Up (PMCF).
The service enables controlled collaborative processing of sensitive health data within isolated and audit-capable project environments aligned with GDPR and institutional information security requirements. The VRE supports isolated project workspaces on shared multi-tenant infrastructure with secure remote access, managed analysis environments, and traceable processing workflows.
VRE services include:
- Secure isolated project workspaces
- Secure data exchange between Charité and external partners
- Trusted Research Environment / Secure Processing Environment and secure collaboration workflows for sensitive health data like imaging, genetic, or clinical data
- Remote Desktop virtual machines
- Managed Jupyter and Linux analysis environments
- GPU-enabled compute resources
- Long-term storage, backup, and recovery mechanisms
- Audit logging and traceability support
- Monitoring and operational oversight
- Guacamole/VPN-based remote access
- Support for automated pseudonymisation and anonymisation workflows
- SOPs, onboarding, and user support
- Project coordination and operational support
- GDPR, MDR, and AI Act support processes
- Collaborative data analysis and digital evidence generation
How can the VRE help you?
The VRE enables secure and GDPR-compliant collaborative research with sensitive human health data that cannot be fully anonymized, including imaging, genomics, clinical, and other highly sensitive biomedical datasets. The platform provides controlled and traceable access to protected data within isolated project environments designed for secure collaborative processing and analysis.
The VRE supports interdisciplinary collaboration between research institutions, healthcare providers, and industrial partners while reducing the need for uncontrolled data transfers and decentralized data handling. Managed analysis environments, secure remote access mechanisms, audit logging, and controlled collaboration workflows support reproducible and secure data processing in compliance-sensitive research settings.
The VRE can additionally support translational and regulatory-oriented activities such as AI system evaluation, PMCF activities, secure secondary use of health data, federated collaborations, and evidence generation for MDR and AI Act related processes.
How is the VRE accessed?
The VRE is primarily accessed through secure remote access mechanisms. Dedicated isolated project spaces are provisioned on Charité-operated infrastructure. Depending on project scope, the service may range from lightweight onboarding and workspace provisioning to fully managed collaborative environments with operational and compliance support.
Typical project durations range from several weeks to multiple years.
Provider Description
Charité operates advanced research and digital infrastructure environments for secure biomedical and clinical data processing in research and translational medicine contexts. The VRE supports interdisciplinary collaboration between clinical, scientific, and industrial stakeholders in compliance-sensitive environments.
Technical Description
The platform is based on shared multi-tenant infrastructure with isolated project environments. Available resources include virtual machines, GPU-enabled compute nodes, storage systems, managed analysis environments, backup systems, authentication and authorization services, and monitoring capabilities.
The environment supports secure remote access, auditability, traceability, and controlled data exchange workflows for sensitive health data processing.
Service Customization
The service can be customized depending on project requirements, including:
- Dedicated or shared compute environments
- GPU-enabled processing
- Long-term storage requirements
- Custom virtual machine sizing
- Federated collaboration scenarios
- Compliance and documentation support
- Enhanced operational support models
- Extended onboarding and training
- Integration with external infrastructures and workflows
Provider & Contact
Indicative prices only; final pricing depends on project scope, duration, storage and compute requirements, GPU usage, operational support level, and governance or compliance requirements.
The Charité VRE (https://vre.charite.de) provides access to a secure and professionally operated research environment for highly sensitive health data, including imaging, genomics, clinical, and other special categories of personal data that often cannot be fully anonymized. The platform combines secure infrastructure, controlled collaboration, managed analysis environments, and governance-oriented operational support within an institutional healthcare and research setting.
Compared to building and operating such environments independently, the VRE enables organizations to access advanced secure processing capabilities, scalable compute and storage resources, collaborative workflows, and compliance-oriented operational processes without the need to establish their own Trusted Research Environment infrastructure.
Pricing includes services such as:
- secure project onboarding and workspace provisioning,
- managed virtual machines and GPU-enabled compute resources,
- secure storage, backup, and long-term archival,
- managed analysis environments and remote access,
- operational administration and user support,
- monitoring, logging, and auditability features,
- governance and compliance support,
- DPIA and GDPR-related support activities,
- project coordination and collaborative support.
Pricing is tailored to project scope, infrastructure utilization, operational support requirements, and governance complexity. The flexible service model allows projects to range from lightweight secure workspaces to large-scale collaborative secure processing environments with dedicated compute, storage, GPU, and compliance support capacities.
Example indicative project scenarios
-
Lightweight secure project workspace with existing infrastructure resources, minimal onboarding, and limited operational involvement:
~4k€–15k€ -
Collaborative secure research project with managed analysis environment, moderate storage and compute requirements, governance support, and operational involvement:
~30k€–85k€ -
Large-scale multi-partner secure data processing environment with GPU-intensive workloads, extensive storage, advanced governance requirements, and extended operational support:
~100k€–250k€+
Reduced pricing may be substantially subsidised through TEF-Health support mechanisms and existing publicly funded infrastructure capacities.
Operational Details
- Adherence to clinical and regulatory standards for device testing in healthcare settings
- GDPR-compliant processing workflows for sensitive human health data
- Support for MDR and AI Act related evidence-generation activities
- Support for Post-Market Clinical Follow-Up (PMCF) activities
- Support for secure secondary use of health data in regulated research contexts
- BSI IT Grundschutz
- Europrivacy
- GDPR
- ISMS
- ISO 27001
- KRITIS