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.
If My Study Includes Approved Drugs, When Do the Risks of Those Drugs Need to Be Disclosed in the Consent Form?
Blog Posts
Caregivers as Research Participants
Blog Posts
Employees as Research Participants
Blog Posts
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
Adults with Limited Capacity to Consent to Research
Blog Posts
What are the requirements for notifications of study closure at research sites?
Blog Posts
Can you use patient Electronic Health Records to identify and recruit subjects?
Blog Posts Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
What questions can be asked when screening patients prior to them signing consent?
Blog Posts