Jan 23, 2013· Advanced Medical Technology Association (AdvaMed) - Comment· FDA-2012-D-0847-0010
Filed on regulations.gov — full text not in the inline record.
FDANonrulemakingFDA-2012-D-0847
Draft Guidance for IRBs, Clinical Investigators, and Sponsors: IRB Responsibilities for Reviewing the Qualifications of Investigators, Adequacy of Research Sites, and the Determination of Whether an IND/IDE is Needed
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Advanced Medical Technology Association filed 1 comment on this docket between Jan 23, 2013 and Jan 23, 2013. 0 other organizations filed here. The comment window closed 4935d ago.
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