Copy this link to access the recording of the session:https://youtu.be/XBprZp2yl6c Informing stakeholder-regulator communication toward medical product development. Objectives: Learn more about ongoing patient engagement efforts to inform regulatory decision making Explore challenges and emerging good practices around the use of patient experience data in regulatory submissions Prioritize Patient Experience Data (PED) challenges and emerging good practices in regulatory communication Understand what areas can help move the needle internally for organizations and externally in collaboration with patient organizations, biopharma and regulators