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.
Ethics in Clinical Research
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts
Series: Ask the IRB & IBC Experts
Adults with Limited Capacity to Consent to Research
Blog Posts
Ethics in Clinical Research
What are the requirements for notifications of study closure at research sites?
Blog Posts
Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
Participant Recruitment
Can you use patient Electronic Health Records to identify and recruit subjects?
Blog Posts
Series: Ask the IRB & IBC Experts
Is informed consent needed for post-market patient registry?
Blog Posts
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
Ethics in Clinical Research
What questions can be asked when screening patients prior to them signing consent?
Blog Posts
Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
Blog Posts
FDA & ICH