Series: Ask the IRB & IBC Experts
At WCG, we get questions about clinical research all the time: from researchers, clinical team members at biopharma companies, and from members of institutional IRBs. We know that for many of the questions, the person asking is not the only one struggling with that issue. We’ve created the Ask the IRB & IBC Experts forum as an immediate and less formal way to share information across the clinical research community. Have a question? Click here to submit your clinical trial ethical or regulatory question.
CenterWatch | Insights
If My Study Includes Approved Drugs, When Do the Risks of Those Drugs Need to Be Disclosed in the Consent Form?
Blog Posts
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Caregivers as Research Participants
Blog Posts
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Employees as Research Participants
Blog Posts
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Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
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Adults with Limited Capacity to Consent to Research
Blog Posts
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What are the requirements for notifications of study closure at research sites?
Blog Posts
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Can you use patient Electronic Health Records to identify and recruit subjects?
Blog Posts
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Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
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What questions can be asked when screening patients prior to them signing consent?
Blog Posts
CenterWatch | Insights