Developing EU methodological frameworks for clinical/performance evaluation and post-market clinical/performance follow-up of medical devices and in vitro diagnostic medical devices (IVDs)

Vergelijkbare regelingen

Dichtstbij qua inhoud — ook over de taalgrens (RVO ↔ EU-calls), via embeddings.

• Generation of scenarios for development, training, virtual testing and validation of CCAM systems (CCAM Partnership) · EU · 87% · open
• EU-wide network of pilot plants and testing facilities, improving SMEs and start-ups' access to scale-up · EU · 87% · open
• Implementation research/real life assessment of existing interventions in women and children’s health · EU · 86% · open
• Improving modes of delivery, deployment, and uptake of vaccines through phase IV/implementation research · EU · 86% · open
• Pre-normative research to develop standards for biodegradability of bio-based products in controlled and in open environments · EU · 86% · open
• Infrastructure-enabled solutions for improving the continuity or extension of Operational Design Domains (ODDs) (CCAM Partnership) · EU · 86% · open