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Gender bias in FDA premarket approval of cardiovascular devices

A systematic review of high-risk cardiovascular devices receiving premarket approval from the U.S. Food and Drug Administration (FDA) found that women were under-represented in the evidence presented to the FDA.  Read more at http://circoutcomes.ahajournals.org/content/early/2011/03/01/CIRCOUTCOMES.110.958215.abstract.

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