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Good morning, everyone, 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, and I lead the scientific evidence generation department at EMA. I am also coordinating our engagement with other decision-makers, including HDA bodies, which is relevant to today's training. We're excited to see around 60 registered participants from the patient and healthcare professional sectors, highlighting the widespread interest in this topic. Notably, some colleagues have joined us for the first time as we introduce HDA Corporation activities in this session.