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FDA Seeks To Include Those Most Affected By Alzheimer’s Disease In The Drug Review Process

The U.S. Food and Drug Administration (FDA) has expanded its Patient Consultant and Patient Representative programs to include individuals in the early stages of Alzheimer’s disease and their caregivers. The FDA made the change in response to a request by the Alzheimer’s Association encouraging the agency to give people directly affected by Alzheimer’s a more active role in the review and approval of new Alzheimer drugs. [click link for full article]

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