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FDA User Fees 2012: How Innovation Helps Patients and Jobs

SueMyrickNC09SueMyrickNC09·100 videos
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Published on Apr 24, 2012

On April 18 at a hearing of the Subcommittee on Health, Energy and Commerce Committee Vice Chair Sue Myrick questioned Dr. Janet Woodcock, Director of the Center for Evaluation and Research at the US Food and Drug Administration, about drug shortages for trauma and critical care patients, and about risk benefit analysis for drugs approved to treat terminal diseases.

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