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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.