Health Policy blog covering advocacy developments and health system initiatives around the world in the areas of:
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Health System Transformation
Interview with Dr. David Bick, Principal Clinician, about Genomics England’s pilot programme to test out the use of genomics in newborn screening in the UK.
Interview with Annie Kennedy, Chief of Policy, Advocacy, and Patient Engagement, about EveryLife’s efforts to enhance the existing newborn screening program in the US.
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.