Health Policy blog covering advocacy developments and health system initiatives around the world in the areas of:
All in Global
Interview with Ann Single, HTAi Patient and Citizen Involvement Interest Group Chair and Patient Voice Initiative Coordinator (Australia), about ongoing gaps in patient and citizen involvement in health technology assessments around the world.
Interview with Flaminia Macchia and Matt Bolz-Johnson, Rare Diseases International, on achieving the UHC vision to leave no one behind as the United Nations adopted a resolution on Persons Living with a Rare Disease and their Families.
Interview with Dr. Karen Facey, lead researcher in IMPACT HTA project on a Framework for Health Technology Assessment (HTA) of Rare Disease Treatments.
Interview with Flaminia Macchia, Executive Director of Rare Diseases International (RDI) about leveraging health policy and frameworks to support improvements in the rare disease space.
