TRAINING CAPSULE I Medical Devices Regulation (MDR): hands-on for paediatrics start-ups

Join this training based on a practical guidance for start-ups to navigate the Medical Device Regulation, illustrated with interactive case studies.

✅ https://eithealth.eventscase.com/EN/innovation_pediatric_capsules_i4kids_eu

Medical Devices Regulation (MDR): hands-on for paediatrics start-ups

Paediatrics start-ups often face significant regulatory challenges (as expressed in our report), with the stricter Medical Devices Regulation (MDR) considered as posing a considerable barrier, especially regarding specific age groups requirements.

Therefore, this capsule adresses the need for practical training on regulatory roadmaps. While a previous capsule focused on the European regulation landscape, this session will provide practical guidance for start-ups to navigate the MDR regulation.

Francisco Rodríguez Gómez, Scientific and Regulatory Affairs Associate Manager at Asphalion, will lead the capsule, guiding you towards a compliance roadmap.
Particularly dedicated to start-ups in the development stage, our expert will share practical knowledge on using the Medical Devices Regulation as an ally, illustrated with interactive case studies, discussing common pitfalls and best practices.
After the presentation, we will open a 15-minutes question and answer session where you will have the opportunity to share your ideas, doubts and opinion on the topic.

🗓️ 27 August 2024

⏰ 13:00 to 14.00

💻 Online

🌐 English

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