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Good morning and welcome to day three of the training session for patients, consumers, and healthcare professionals involved in medicines regulatory activities. My name is Michelle Belkin from the EMA's scientific evidence generation department. I coordinate our engagement with decision-makers such as HDA bodies. Today’s training reflects a significant interest in this topic, with around 60 registered participants, including patients and healthcare professionals. Additionally, some colleagues have joined us for this session as it marks the first time we are discussing HDA Corporation and HDA activities. I'm excited to have so many participants involved.