Canipus is where the world's healthcare innovations live — medical devices, drugs, vaccines, biotech, robotics — each shown with its verified regulatory status. We start at the world's medical expos, and any innovator can publish to Canipus, with every claim cross-checked against FDA, CDSCO, EMA, and clinical trial registries.
Innovations reach Canipus from the world's medical expos — and directly from innovators themselves. Every one passes through the same disciplined pipeline before it's published.
We cover medical expos worldwide as accredited media — and any innovator, from medical-device makers to pharma, biotech, and robotics, can submit their innovation directly.
AI reads every video, brochure, and submission, and extracts the structured claims — company, product, indication, and the regulatory stage being claimed.
AI cross-checks each claim against FDA, CDSCO, EMA, and clinical-trial registries, pulling the real status automatically — confirmed by our editorial team.
The innovation goes live with a clear verified status badge — organized by disease and country, with alerts when its regulatory status changes.
Whether an innovation comes from an expo or is submitted by the innovator directly, the rule is the same. Every product, drug, device, and therapy carries a verified badge linking to its actual regulatory record.
From early research to FDA approval — and recalls, withdrawals, and failed trials too. Honest tracking, including what didn't work.
Healthcare innovation matters to more than one role. Canipus personalizes what you see based on who you are and what you're tracking.
Join the waitlist for early access. We'll cover what's happening at the world's medical expos — verified at the source, delivered to you weekly.