Today’s post is by Michael Happich (Director HTA BioMeds, Canada & Europe) at Eli Lilly & Robin Thompson (Director, EU+ Value and Market Access) at Biogen International. They will introduce us to the need to consider differing perspectives and subsequently the need for broader engagement in the creation of conditions for an open collaboration among stakeholders that yields consensual and efficient uses of real-world evidence for the benefit of AD patients and their caregivers.
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