We help medical device and pharma companies generate real-world evidence by collecting outcomes directly from patients, with around 85% engagement. The data is live and audit-ready, and it can be used for market access, reimbursement and marketing, with post-market surveillance covered too. We work with hardware, software and AI devices. At MEDICA we want to meet device and pharma companies, distributors, and market access teams who need real-world evidence.
Cardiology/Vascular DiseasesDental & Oral HealthDermatologyDiagnosticsEndocrinologyGastroenterologyGenetic DiseaseHematologyHepatologyImmunologyInfections and Infectious DiseasesInternal MedicineMusculoskeletalNephrologyNeurologyNutrition and Weight LossObstetrics/GynecologyOncologyOphthalmologyOrthopedics/Orthopedic SurgeryOtolaryngologyPharmacology/ToxicologyPodiatryPsychiatry/PsychologyPulmonary/Respiratory DiseasesRare DiseaseRheumatologyTraumaUrologyVaccines
ROBOTICS AND AUTOMATION
AI guided robotics and automationSensor networksData processing and analysis
INTELLECTUAL PROPERTY, LEGAL AND FINANCIAL SERVICES
Regulatory affairs
LIFE SCIENCE
e-Health and ICT solutionsHospital and Care equipmentMedical ServicesOperating technology and equipmentPhysiotherapy, Orthopaedic TechnologySurgery and EndoscopyTherapy and physical medicine
Real-world patient outcomes for PMCF, PMS & market access. ~85% patient engagement, live and audit-ready. Helping medtech, pharma & regulatory teams navigate MDR compliance with evidence that's actually useable - not just a regulatory tick box.