HTA decision-making for drugs for rare diseases: comparison of processes across countries.
Tania StafinskiJudith GlennieAndrea YoungDevidas MenonPublished in: Orphanet journal of rare diseases (2022)
Based on the collective findings from all components of the project, seven recommendations for possible action in Canada are proposed. These focus on defining "appropriate access", determining when a "full" HTA may not be needed, improving coordination among stakeholder groups, developing a Canadian framework for Managed Access Plans, creating a pan-Canadian DRD/rare disease data infrastructure, genuine and continued engagement of patient groups and clinicians, and further research on different decision and financing options, including MAPs.