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"Clinical Evaluation of Orphan Medical Devices – EU Regulatory Guidance"

Join us in this informative session and learn about the orphan medical devices European guidance.
i4KIDS4RARE Training Capsule

Register here: https://www.eventbrite.es/e/i4kids-i-i4kids4rare-training-capsule-tickets-1262374729799?aff=oddtdtcreator

i4KIDS – i4KIDS4RARE Training Capsule: “Clinical Evaluation of Orphan Medical Devices – EU Regulatory Guidance”

Join us for our next training capsule with Dr. Gearóid McGauran, Medical Officer at the Health Products Regulatory Authority (HPRA), Ireland. Dr. McGauran was the lead author of MDCG 2024-10, the key EU guidance on orphan medical devices, and is a member of the MDCG Orphan Device Taskforce and CIE Working Group.

📅 Date: 27th March
⏰ Time: 13:00 – 14:00 (CET)
💻 Format: Online

Dr McGauran will outline key considerations for clinical evidence generation for orphan devices, including clinical investigations and EU regulatory support, based on MDCG 2024-10.

Don’t miss this expert-led session on EU regulatory pathways for orphan medical devices!

 

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