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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. I’m Michelle Belkin from the EMA's scientific evidence generation department, coordinating our engagement with various decision-makers, including HDA bodies. Today’s training is significant, with approximately 60 registered participants from both patient and healthcare professional backgrounds, highlighting the broad interest in this topic. It’s also notable that some additional colleagues joined this session, as it marks the first instance of HDA collaboration and activities. I’m excited to share valuable insights during our time together.