MDR and drugs for pediatrics: how to navigate within the regulatory ocean?
What is the regulatory roadmap for paediatric medical devices and drugs before they can be marketed?
i4KIDS I i4KIDS-EUROPE Training Capsule dedicated to learn how to drive innovation through regulatory roadmaps for both Medical Devices Regulation (MDR) and Drugs Regulation with Xavier Luria, a seasoned expert in Medical Devices and Drugs regulation with extensive experience at European Medicines Agency, illuminates strategies to reflect on the regulatory landscape in Europe.
SESSION IN ENGLISH
Related News
Featured
The second edition of the Paediatric Investment Forum will be held on 17 September 2026 in Helsinki, bringing together European startups, investors and ecosystem leaders to accelerate innovation in paediatric and maternal health.
Featured
i4KIDS visited Alder Hey Children’s Hospital in Liverpool to learn about its paediatric innovation model. Over two days, the team explored the hospital’s innovation spaces, took part in workshops on design thinking, artificial intelligence and innovation culture, and attended the Alder Hey Innovation Celebration Conference, where various perspectives and initiatives in paediatric health innovation were presented. The visit provided insight into methodologies and approaches used in other healthcare systems and opened new opportunities for international collaboration.
Featured
i4KIDS has opened the call for the 3rd edition of its Acceleration Programme 2026, a six‑month initiative designed to fast‑track early‑stage innovations in fetal, paediatric and maternal health. The programme will select seven high‑potential projects and provide training, mentoring, expert consultancy and pitch preparation, culminating in a Demo Day in Barcelona in November 2026. Applications are open until 12 April 2026.