Healthcare and life sciences run on regulated data. MFD builds the platforms that connect clinical, claims, real-world evidence and operational data -- and ships domain LLMs that augment clinicians, scientists and operations teams without compromising patient safety.
MFD combines enterprise data infrastructure, AI automation and governed intelligence into one operational system designed for modern enterprises.
Unified records, longitudinal patient views and care orchestration
Automated submissions to FDA, EMA, MHRA and equivalents
Diagnostics support, length-of-stay and readmission models
Cohort discovery, trial design and post-market surveillance
Molecule discovery, simulation and quantum-assisted simulation pilots
MFD combines enterprise data infrastructure, AI automation and governed intelligence into one operational system designed for modern enterprises.
For clinical and operational analytics
For regulated metadata management
For domain clinical and pharmacovigilance LLMs
HIPAA, HITRUST, GDPR, EU AI Act, FDA 21 CFR Part 11, GxP, GAMP 5.
Engagements span global pharma, payers and providers.
Specific references available under NDA. Contact our regional directors for detailed case studies.