DorothAI™ is a governance platform that lets healthcare teams deploy and manage AI safely within their existing workflows.

DorothAI™ monitors patient safety risks in real-time providing alerts to prevent patient harm while maintaining full compliance.

Starting with cardio-oncology safety during chemotherapy, we bridge the gap between static models and high-risk clinical workflows.
DorothAI™ improves outcomes for 100K+ patients annually receiving HER2-targeted therapy across major markets.
Standard AI models lack the clinical guardrails required for reliable medical decisions.
Regulatory complexity often prevents teams from using AI to improve patient outcomes.
AI is being adopted. It is not safe to deploy.
Healthcare systems are using AI without structural safeguards. Many tools aren’t designed for high-risk clinical environments, where accountability is non-negotiable.
Cancer treatments save lives, but can cause permanent heart damages. Current monitoring is reactive, manual, and prone to significant high variability.
Models trained on static datasets fail to account for individual patient trajectories. Without real-time governance, static AI is a clinical liability.
We don’t just provide a model; we provide a governed execution environment for medical intelligence.

Deep integration into the patient’s oncology journey, capturing nuanced real world data.

Task specific, highly specialised models designed for predictive accuracy in cardiotoxicity.

Auditable, printable results with built in human in the loop validation checkpoints.
We don’t just provide a model; we provide a governed execution environment for medical intelligence.

Preventing complications from intensive treatments through predictive, surveillance and daily safety alerts.
Moving to tailored safety monitoring that maps individual patient risks in real time.
Providing healthcare teams with governed insights to adjust patient care before Issues arise.
Deploying AI with confidence through a shared layer of governance and safety

Deploy AI safely across your organization while maintaining full clinical control:

Built evidence with governed data and traceable models for clinical research:

Accelerate development with trusted outcomes and continue safety monitoring:
Inquire about our early-adopter pilot program or request technical specifications.
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