Healthcare
Enterprise AI foundations for regulated, data-sensitive clinical and operational workflows.
Overview
Clinical and operational AI lives or dies on governance. We build enterprise AI foundations for regulated, data-sensitive workflows – accountable, auditable, and scoped to a guaranteed outcome.
Accelerators
Accelerators for Healthcare.
Software Testing
Parikshan
AI across the software testing lifecycle, from authoring to release.
LifecycleAI in software testing
Production Execution & Traceability
Anvaya™
Every order traced from raw material to finished unit, in one genealogy view.
Both waysgenealogy from raw material to finished unit
Design Risk & DFMEA
Tatvam™
The whole failure-mode workflow in one control room, auditable end to end.
Initial vs residualRPN compared in a sortable risk register
Regulatory Change Intelligence
Parivart™
Know which products a new rule touches, before the deadline finds you.
Mappedrule to product, market, and process
Demand & Inventory
Sanchay™
Forecast demand, size inventory, and reorder before the shelf empties or the batch expires.
Per SKUforecasting with tracked accuracy
Healthcare Governance
Drishti™
One live console for healthcare compliance, security, and clinical AI oversight.
Four frameworksmonitored continuously, not annually
Autonomous Security Testing
Vedha™
Authorized penetration testing on a release cadence, not a quarterly one.
Continuoustesting cadence instead of quarterly
Use cases
The work we run in healthcare.
25 modelled workflows, each with the steps it runs and the outcome it moves.
Healthcare
Engineering
Automated Synthetic Test Data Generation & PII Masking for Healthcare
A HealthTech platform processing electronic health records (EHR) and insurance claims under strict HIPAA privacy compliance.
- HIPAA-compliant testing environment with zero real patient data
- 100%HIPAA-compliant testing environment with zero real patient data
- test data preparation time cut
- 2 weekstest data preparation time cut
Healthcare
Quality & Compliance
Instant Recall & Targeted Population-at-Risk Isolation for Medical Devices
An ISO 13485-certified medical device manufacturer produces portable patient monitoring units containing sensitive microprocessor boards and rechargeable lithium power modules. Production involves high-volume SMT PCBA assembly followed by multi-stage device integration and burn-in testing.
- quarantined product volume drops
- 95%quarantined product volume drops
- recall investigation and containment plan generation completed
- 15 minutesrecall investigation and containment plan generation completed
Healthcare
Quality & Compliance
Serialization Compliance for Regulated Medical Device Production
A medical device manufacturer must maintain unit-level serialization and device history records across three production lines to satisfy regulatory requirements.
Healthcare
Quality & Compliance
Global Medical Device Portfolio Compliance & EU MDR / FDA Regulation Updates
A global medical technology manufacturer with a portfolio of 450 class II and class III cardiovascular and orthopedic devices marketed across 35 countries.
- regulatory change detection and impact analysis time cut
- 6 weeksregulatory change detection and impact analysis time cut
- reduced regulatory consulting and contractor spend
- $480,000reduced regulatory consulting and contractor spend
Healthcare
Quality & Compliance
Biopharmaceutical Multi Market Labeling & Safety Guideline Harmonization
A biopharmaceutical enterprise marketing monoclonal antibody therapies and oncology therapeutics across North America, Europe, Asia Pacific, and Latin America.
- time compliance with statutory safety labeling updates
- 100%time compliance with statutory safety labeling updates
- label discrepancy identification cycle time reduced
- 30 dayslabel discrepancy identification cycle time reduced
Healthcare
Quality & Compliance
Cross Functional Regulatory Change Command Center & Audit Readiness
An enterprise industrial conglomerate managing 6 operating divisions across aerospace, medical, automotive, and heavy energy infrastructure.
- regulatory audit preparation time reduced
- 3 weeksregulatory audit preparation time reduced
- successful audit outcomes with zero major non conformances
- 100%successful audit outcomes with zero major non conformances