MFD builds platforms that connect clinical, claims and real-world evidence 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 regulated healthcare and life sciences organisations.
Unified records, longitudinal patient views and care orchestration across FHIR and legacy systems.
Automated submissions to FDA, EMA, MHRA and equivalents with 21 CFR Part 11 audit trails.
Diagnostic support, length-of-stay and readmission models with explainability and drift monitoring.
Cohort discovery, trial design feasibility and post-market surveillance at scale.
Molecule discovery, simulation and quantum-assisted modelling pilots for R&D acceleration.
MFD combines enterprise data infrastructure, AI automation and governed intelligence into one operational system designed for modern healthcare and life sciences 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.
MFD has delivered AI and data platforms to global pharmaceutical companies, healthcare payers and provider networks across the US, Europe and Asia. Specific references available under NDA. Contact our regional directors for detailed case studies.
Specific references available under NDA. Contact our regional directors for detailed case studies.