A long-awaited report on the 2004 Food and Drug Administration decision to reject an application to allow easier access to the "morning after pill" concludes that the decision was highly unusual, was made with atypical involvement from top agency officials, and may well have been made months before it was formally announced.
The draft report by the Government Accountability Office, requested by Congress in the summer of 2004, is to be finalized and made public by the end of the month. But some congressional staffers have been briefed on its conclusions in recent weeks, and some were allowed yesterday to read the findings.
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