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Five minutes with Vee Mapunde on: the growing influence of patient advocacy groups in Early Access Programmes

Five minutes with Vee Mapunde on: the growing influence of patient advocacy groups in Early Access Programmes

We had a chat with Vee Mapunde, Associate Consumer Lead at the National Cancer Research Institute (NCRI) on the role of patient advocacy groups in the Early Access Prorammes landscape, their missions and the tools they have to fulfill them, ahead of the Early and Managed Access Programmes conference (24th-26th October 20170. The power is now shifting towards the patients, so what impact does this have on patient advocacy groups?


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