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
May I pay a physician for referring a patient to our study?
Blog Posts
WCG Clinical | Insights
Regulatory Challenges in Pediatric Drug Development: The European Perspective
Blog Posts
WCG Clinical | Insights
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts
WCG Clinical | Insights
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Blog Posts
WCG Clinical | Insights
What are the regulations for training home health individuals who are working remotely to collect study data?
Blog Posts
WCG Clinical | Insights
Should Consent Form updates be aligned with Investigator Brochure updates, or wait for next Protocol amendment?
Blog Posts
WCG Clinical | Insights
What are the requirements for parental permission (consent) in studies involving children?
Blog Posts
WCG Clinical | Insights
How do I handle a deviation in the use of blood specimens collected outside the timeframe?
Blog Posts
WCG Clinical | Insights
Is it possible to make a PI’s name or institution confidential on a consent form?
Blog Posts
WCG Clinical | Insights