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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, and I'm coordinating our engagement with decision-makers, including HDA bodies. We're thrilled to have around 60 registered participants here, highlighting the significant interest in this topic. Additional colleagues have joined the session today, marking the first time we are incorporating HDA activities into our discussions.
