2) HORIZON-HLTH-2026-01-IND-03 – Regulatory science to support translational development of patient-centred health technologies

SUBMED can contribute through its expertise in ISO 13485 quality management systems, product lifecycle management, sterilisation and validation, and preclinical evidence generation, providing an industrial regulatory science perspective. Within the project, SUBMED can deliver real-world industrial case studies illustrating how innovative patient-centred health technologies can be optimised for regulatory compliance, risk management and patient safety from early R&D stages through to market access. Its contribution will focus on translating regulatory science concepts into practical, implementable approaches that are directly relevant to industry and regulatory stakeholders.