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National Council on Patient Information & Education

The National Council on Patient Information and Education (NCPIE) is a collaborative project of over 125 diverse organizations to better inform the public on appropriate use of medicine and improve public health.  Diane Dorman, Vice President for Public Policy, is a member of the Board of Directors for the National Council on Patient Information and Education.  In this role, she continues to advocate for the rare disease community on matters relating to prescription medicine usage within the larger context of public health. Visit the National Council on Patient Information and Education (NCPIE)’s website.

 

 
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