Published in Blood Weekly, July 15th, 2004
The blinded review of data by an independent panel of experts was agreed upon with the U.S. Food and Drug Administration (FDA) as a next step in the U.S. regulatory submission for the Intercept Blood System for platelets.
The analysis of primary patient records performed under the direction of an independent contract research organization...
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Source: Blood Weekly (2004-07-15)
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