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Why Is It Still So Hard for People to Get Their Health Data?
Patients are the source, active or passive, of most of the data driving discovery and innovation
in biomedical R&D and improvements in care.
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Bridging the Non-Profit and For-Profit Divide for Research: Maximizing Your Partnerships to Enhance Patient Engagement (Invite only)
Industry and patient organizations can work together to streamline the process of acquiring and
incorporating patient input in biomedical research.
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Center for the Future of Aging Advisory Board Breakfast (Invite only)
The Milken Institute Center for the Future of Aging Advisory Board is comprised of the Leadershi
p Council and the Academic and Policy Council, influential leaders and experts working to ensure that individuals, institutions, and societies are prepared f
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Cell and Gene Therapies: Are We Setting the Right Expectations? (Invite only)
Cell and gene therapies are generating excitement for their potential to treat diseases more pre
cisely, but are expectations for these therapies realistic?
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Accelerating Access to Lifesaving Treatments and Cures: Insights from FDA's Expedited Review Programs
The Food and Drug Administration's (FDA) expedited review processes have been instrumental in ma
king treatments available for individuals living with serious illnesses.
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Prioritizing Accountability for Health Equity (Invite only)
Without accountability to prioritize health outcomes of minority populations, there cannot be tr
ue progress toward health equity. Many biomedical investigators recognize the paramount importance of health equity, yet progress has been slow.
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FasterCures Board Meeting (Invite only)
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Technology Solutions for Food Is Medicine Prescriptions Lunch (Invite only)
With health-care-related costs continuing to rise, it is imperative to fund population health st
rategies that use food and nutrition as tools to treat and prevent costly diet-related diseases, as well as to feed food-insecure populations.
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