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Maria Hardin
Vice President, Patient Services
National Organization for Rare Disorders

Maria Hardin, serves as Vice President of Patient Services for the National Organization for Rare Disorders (NORD), the primary consumer federation responsible for enactment of the Orphan Drug Act. Ms. Hardin’s 21-year tenure at NORD includes oversight of strategic direction and operation of NORD’s 38 medication and health insurance co-payment assistance programs. She is frequently invited to serve on industry roundtables to address patient access issues that are an integral part of the drug development process.

Learn more about Maria Hardin

Programs:
05/27/2008 - Access to Care: Insurance and Reimbursement Support Programs for New PKU Treatments Program Details >>
05/27/2008 - Acceso a la atención médica: Programas de apoyo para obtener la cobertura del seguro médico y reembolsos para los nuevos tratamientos de la fenilcetonuria Program Details >>

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