Welcome to HubMed at CPHI Milan 2026!
Turn EU MDR Complexity into Clinical Confidence. See how Medea™ cuts CER drafting time by up to 70%.
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Why RA/QA Leaders Choose Medea™
70% Time Savings
Automates literature screening across online scientific databases, recovering ~30 hours per Clinical Evaluation Report.
100% Audit-Ready
Generates documentation natively structured according to EU MDR 2017/745 Annex XIV requirements.
Zero Regulatory Blind Spots
Ensures verifiable, traceable literature appraisals to eliminate Notified Body objections.
📍 Visiting the Start-Up Market Zone?
Come meet the HubMed team in person:
CPHI Milan (October 6–8)
🏢 HubMed Booth: Stand 8S114
📍 Zone: Start-Up Market