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
May I pay a physician for referring a patient to our study?
Blog Posts
CenterWatch | Insights
Regulatory Challenges in Pediatric Drug Development: The European Perspective
Blog Posts
CenterWatch | Insights
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts
CenterWatch | Insights
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Blog Posts
CenterWatch | Insights
What are the regulations for training home health individuals who are working remotely to collect study data?
Blog Posts
CenterWatch | Insights
What are the requirements for parental permission (consent) in studies involving children?
Blog Posts
CenterWatch | Insights
How do I handle a deviation in the use of blood specimens collected outside the timeframe?
Blog Posts
CenterWatch | Insights