EU MDR / IVDR Compliance Assistant
AI-powered guidance for clinical trial compliance under EU MDR and IVDR. Get a personalised roadmap, generate regulatory documents, and estimate study budgets — instantly.
Regulatory Chat
Ask questions about EU MDR / IVDR requirements. Get instant, context-aware answers based on official EU regulatory guidance.
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Compliance Roadmap
Answer a short questionnaire about your study. Get a personalised step-by-step regulatory roadmap with timelines and citations.
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Budget Estimator
Complete the study wizard and get a personalised cost estimate — CRO vs. self-managed, with EU country-specific breakdowns.
Estimate costs →