The European Medicines Agency (EMA) engagement framework aims to
- Facilitate participation of patients and consumers in regulatory activities all along the entire lifecycle of medicines;
- Foster the development of guidance and methodologies to increase collection and use of relevant patient experience data in the context of regulatory decision making;
- Ensure that patients, consumers and their representative organisations are consulted and, where appropriate, involved in the development of EMA policies and plans
- Support optimal participation of patients and consumers in EMA activities by establishing a training programme.
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