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DewDiligence

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Re: randychub post# 74

Friday, 03/26/2004 11:32:18 AM

Friday, March 26, 2004 11:32:18 AM

Post# of 9289
No matter how diligent a job is done gathering the data, after six-plus years not every patient will be accounted for. (This was confirmed in the CC.) The FDA may decide to ignore the missing data points, but requiring a small prospective trial seems like a reasonable compromise under the circumstances.

“The efficient-market hypothesis may be
the foremost piece of B.S. ever promulgated
in any area of human knowledge!”

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