We are thrilled to announce that HubMed will be at CPHI Milan (October 6–8) as an Official Sponsor!
As global regulatory demands intensify across MedTech, Nutraceuticals, and Life Sciences, keeping pace with compliance while scaling R&D has become one of the industry's greatest bottlenecks. At CPHI Milan, HubMed is stepping onto the stage to show how AI-assisted SaaS solutions are reducing these friction points for good.
Here is what we are bringing to Milan—and where you can find us.
📍 Where to Find Us
Come visit the HubMed team during the event to chat with our leadership and product experts:
🏢 HubMed Booth: Stand 8S114
📍 Zone: Start-Up Market
⚡ Beyond Slides: See Medea™ in Action Live at Our Booth
Forget canned slide decks. At the HubMed booth, we are giving attendees an interactive, hands-on look at Medea™, our AI-assisted platform built specifically to accelerate Clinical Evaluation Reports (CERs) under EU MDR 2017/745.
CER workflows are notoriously research-intensive, often swallowing dozens of hours of expert time in literature screening and data extraction. Medea™ transforms this process by seamlessly handling:
AI-Assisted Systematic Literature Searches across PubMed and other scientific online databases.
AI-Assisted Evidence Appraisal weighted for scientific relevance and bias.
Annex XIV-Native Documentation ensuring 100% audit-readiness.
📊 The Numbers Speak for Themselves
70% time reduction in the research-intensive phase of CER drafting.
~30 hours recovered per clinical evaluation report.
€16,344+ minimum annual savings for a CRO producing just 2 CERs per month—starting from month one.
At our booth, you can test Medea™ on real workflows, ask the tough regulatory questions, and see firsthand what a 70% time saving looks like in practice.
🎙️ Don't Miss Our Panel Session: Nutraceuticals: Scaling Without Breaking Supply
In addition to our live booth demonstrations, HubMed will be contributing to an expert panel on the Supply & Formulation Excellence stage.
📅 Date & Time: October 8th | 10:30 AM – 11:15 AM
📍 Location: Stage Hall 2 (Stand 2A132)
Why Regulatory Compliance is the New Supply Chain Bottleneck
While nutraceuticals are growing faster than almost any adjacent health category, regulators in the US and EU are rapidly tightening scrutiny—from GRAS reform to stricter marketing enforcement. At the same time, modern consumers no longer accept unverified claims; they demand hard proof of bioavailability and clinical efficacy.
During this session, we will discuss how companies can scale their products without running into regulatory dead ends, and how AI-assisted scientific appraisal bridges the gap between raw ingredient supply and bulletproof market claims.
📅 Book Your Live Demo Ahead of Time & Claim a Free Visitor Pass
CPHI Milan is one of the largest gatherings in the global pharmaceutical and health industry. To guarantee dedicated, one-on-one time with our executive and technical team, we recommend reserving your demo slot in advance.
How to connect with us:
Reserve a Meeting: Visit our Contact Page to schedule your personalized demo.
Visit Stand 8S114: Stop by our booth in the Start-Up Market Zone anytime from October 6 to 8.
Claim Your Visitor Pass: We have reserved a limited number of complimentary CPHI passes for regulatory, QA, and R&D leaders—available on a first-come, first-served basis.
Whether you are looking to streamline your EU MDR clinical evaluation pipeline or elevate the scientific evidence backing your health products, we look forward to meeting you in Milan!
Claim your free CPHI pass & reserve a 1-on-1 demo with our team