Digital Health Compliance Tracker

Automated monitoring of FDA, MHRA, and EU regulatory changes for Software as a Medical Device (SaMD) teams.

Automated scans of FDA RSS feeds, MHRA updates, and EU medical device portals every 24 hours.

LLM-powered parsing delivers impact levels, affected roles, and required actions in plain language.

Engineers, product managers, and compliance leads get actionable summaries — no legal fine print.