Implement advanced LLMs and AI agents to accelerate literature synthesis, data mining, and hypothesis validation for clinical research teams.
Navigate complex EU requirements including GDPR, MDR, and the AI Act to ensure your research can safely reach deployment.
Transform research prototypes into scalable, reliable production systems with proper monitoring and maintenance.
How CaraOmics.ai delivers exceptional value throughout the research-to-deployment journey
Confidently address the requirements of GDPR, MDR, and the emerging AI Act with guidance from experts who understand both the technical and regulatory aspects.
Bridge the gap between promising research prototypes and production-grade systems that can reliably serve real-world healthcare environments.
Leverage specialized cloud and AI systems designed specifically for the unique requirements of sensitive healthcare data and clinical research workflows.
Bridging the gap between research breakthrough and patient impact with specialized expertise.
CaraOmics.ai was founded to solve a critical problem in medical research: brilliant discoveries that remain trapped in academic settings because research teams lack the specialized expertise to navigate AI productization, cloud architecture, and EU regulatory compliance simultaneously.
Led by Colm Coffey, who combines a unique background in biomedical engineering, medical device cybersecurity, and advanced AI systems, CaraOmics.ai serves as the technical bridge between research breakthrough and patient impact. As WP5 technical lead for the EU Horizon project Parkstwin, Colm has firsthand experience guiding complex medical AI projects through the entire lifecycle—from prototype to regulatory-compliant deployment.
This rare combination of domain expertise allows CaraOmics.ai to address the complete challenge: not just the technical implementation, but the regulatory strategy, security architecture, and compliance frameworks that determine whether innovative research becomes accessible healthcare solutions or remains in development indefinitely.
Supporting research teams through the complete journey from discovery to deployment.
Research teams often struggle to scale promising AI prototypes beyond proof-of-concept. CaraOmics.ai designs and implements complete pipelines that transform experimental models into production-ready systems, handling everything from literature synthesis and data mining to hypothesis validation using advanced LLMs and AI agents.
Moving sensitive medical data to the cloud requires specialized expertise in both AWS services and EU healthcare regulations. CaraOmics.ai designs and deploys compliant environments using EC2, S3, SageMaker, and Bedrock, with security frameworks specifically aligned with GDPR, data sovereignty, and emerging AI Act requirements.
Researchers need accessible ways to explore complex datasets and validate findings without becoming data engineers. CaraOmics.ai creates intuitive dashboards that allow research teams to derive insights, explore knowledge, and communicate findings effectively to both technical and non-technical stakeholders.
The gap between a working prototype and a reliable production system is where many research projects fail. CaraOmics.ai implements comprehensive testing, monitoring, and operational frameworks that ensure AI systems remain accurate, efficient, and maintainable in real-world environments.
EU regulatory requirements for AI in healthcare are complex and evolving. CaraOmics.ai conducts comprehensive compliance audits against GDPR, MDR, and AI Act requirements, providing clear roadmaps for achieving regulatory readiness before deployment or funding reviews.
Implementing Large Language Models and AI agents to accelerate research, automate repetitive tasks, and provide valuable insights from complex biomedical datasets and literature.
Navigating the complex landscape of EU AI requirements and medical data handling regulations.
Bridging the divide between research code and production-grade systems that can scale reliably.
Meeting strict compliance standards that often slow development and deployment timelines.
Successfully integrating AI solutions with existing clinical workflows and legacy systems.
Accessing specialized cloud and AI expertise without expanding permanent staff.
Real-world experience with regulatory requirements and clinical workflows that inform technical decisions.
Deep knowledge of GDPR, MDR, and emerging AI Act compliance requirements for healthcare applications.
Hands-on experience with LLMs, AI agents, and production ML systems for healthcare applications.
Technical leadership in EU Horizon medical AI projects with demonstrated success in deployment.
Complete support from research prototype to regulatory-compliant deployment and maintenance.
Contact CaraOmics.ai to discuss how AI and secure cloud infrastructure can advance your research and meet critical EU compliance needs like GDPR and the AI Act.
For more information about our services or to discuss your project, please email us directly at:
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You can also call us at: +31 68 192 2398
