Gastroenterology
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Series: Ask the IRB & IBC Experts
Is it possible to make a PI’s name or institution confidential on a consent form?
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WCG Experts to Lead Nine Educational Sessions at the PRIM&R 2019 Advancing Ethical Research Conference
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Series: Ask the IRB & IBC Experts
What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
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Questions on Using Generic Recruitment Flyers at Clinical Trial Sites
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What is the IRB’s responsibility for the review of updated Investigator Brochures?
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Ethics in Clinical Research
If a Subject’s Care Is Divided Equally Between Two Caregivers, Who Should Sign Caregiver Consent?
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Regulatory Compliance
Can we charge a subject for a diagnostic test not done as part of the IRB approved protocol?
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Is it ethical to pay subjects for referring friends to a clinical research site?
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Regulatory Compliance
How should a site document a missing signature on a HIPAA authorization form?
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Clinical Trial Safety