Regulatory intelligence for AI in life sciences

TamRx is a regulatory intelligence platform for artificial intelligence used in life sciences. It helps medical device companies, healthcare-AI teams and pharmaceutical organisations understand the regulatory consequences of changes across the AI lifecycle — retraining, fine-tuning, model updates, data changes and drift — across the EU AI Act, EU MDR and IVDR, the UK MHRA regime and the US FDA regime.

TamRx is not a chatbot, a consultancy or a document repository. It is a structured workbench: it classifies a regulatory question, reasons along a curated consequence structure, simulates the perspectives of the relevant reviewers, and returns a consistent, source-cited assessment designed for review by a qualified person.

The platform exists because the question it answers — what happens to your regulatory obligations when your AI changes — is slow, expensive and expert-bound today, and answered poorly by generic tools. TamRx makes that reasoning fast, structured and transparent, while keeping a qualified human accountable for every decision.