FDA is holding a public hearing on...

FDA is holding a public hearing onward March 21 to examine whether investigators should project reports to IRBs of all adverse results related to a clinical studious mood Current policy requires researchers to report all "unanticipated problems" Unfortunate y this means a certain IRBs receive thousands of reports, many of them unclear and incomplete.
Last July (2004) Ernest Prentice, Chair of the HH Secretary's Advisory Committee in succession Human Research Protections (SACHRP/outlined this moot point in a letter to HH secretary Tommy Thompson Prentice noted that a certain quantity of IRBs received more than

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