Series: Ask the IRB & IBC Experts
WCG’s IRB & IBC Review professionals 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 built this forum as an immediate and less formal way to share information across the clinical research community.
WCG Clinical | Insights
Post Study Activities Requiring IRB Review
Blog Posts
WCG Clinical | Insights
What is the WCG IRB’s current process for reviewing research involving children as subjects that is not otherwise approvable by an IRB?
Blog Posts
WCG Clinical | Insights
Caregivers as Research Participants
Blog Posts
WCG Clinical | Insights
Employees as Research Participants
Blog Posts
WCG Clinical | Insights
Should a Protocol Amendment be Submitted in Advance of Consent Form Changes?
Blog Posts
WCG Clinical | Insights
Which comes first – IRB or IBC approval?
Blog Posts
WCG Clinical | Insights
Is special safety equipment required for IBC approval?
Blog Posts
WCG Clinical | Insights
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
WCG Clinical | Insights
Adults with Limited Capacity to Consent to Research
Blog Posts
WCG Clinical | Insights