Internal Review Boards
RSSArticles
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When protocol changes, updated consent needed
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Points to consider during continuing review
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On-line conference trains researchers
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Adverse event reporting often creates confusion, conflicts over when and how
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Have book, will study
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Spotlight on Compliance: Off-label use differs from investigational use
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Using informed consent forms vs. progress notes
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Clinical trials harmed by lack of informed consent
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Should IRBs standardize payments to subjects?
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Key finance question: Is relationship covered?