Fondazione RIC collaborates with life sciences, medical device, digital health, and technology companies not only as an independent scientific partner, but also as a qualified provider of specialized clinical research services. In addition to enabling investigator-initiated and academically driven studies, Fondazione can directly deliver operational, regulatory, and digital services across the full study lifecycle. These include protocol development, regulatory and IRB submissions (EU CTR, MDR, ISO 14155), study governance and sponsor oversight, eCRF design and validation, data management, statistical support, monitoring coordination, vendor qualification, and publication planning…
All activities are performed within a robust non-profit governance framework that guarantees scientific independence, data integrity, and compliance with GCP, GDPR, and applicable regulatory standards. This integrated model allows companies to outsource critical study components to a trusted academic foundation, generate high-quality clinical evidence, and support innovation and regulatory strategies while preserving transparency, ethical rigor, and clear separation from commercial influence.