Medical Device Registries: Bridging the Gap Between Device Performance in Clinical Trials and Their Use in Routine Practice
Medical Device Registries: Bridging the Gap Between Device Performance in Clinical Trials and Their Use in Routine Practice
1 PagesThis fact sheet highlights IQVIA’s MedTech registries, designed to evaluate device safety, effectiveness, and value in real-world settings. Registries meet multi-stakeholder needs—patients, physicians, regulators, industry, and payers—by informing decisions, monitoring safety, and securing reimbursement. IQVIA delivers design excellence, flexible data collection, enriched study designs, and registry linkages for cost-efficient execution. Regulatory alignment spans FDA CDRH, EU MDR/IVDR, and ISO 14155:2020. Leveraging NextGen technologies, digital platforms, and global-local expertise, IQVIA enables faster recruitment, direct-to-patient approaches, and smarter evidence generation, bridging the gap between trial performance and routine practice outcomes.
