FDA and the Office for Human Research Protections (OHRP) issued a 16-page draft guidance, entitled “Key Information and Facilitating Understanding…
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By James M. DuBois, DSc, PhD There is currently nothing to prevent qualitative researchers from dumping data that are sensitive…
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By Emily E. Anderson, Stephanie Solomon Cargill, and Ryan Spellecy Engaging communities in research beyond mere enrollment is not new…
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Promoting Evidence-Informed Consent Practices: Focus Groups with IRB Directors, Chairs, or Delegates
Does your IRB review biomedical clinical trials? If so, we are NIH-funded researchers at Washington University in St. Louis who…
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