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.
Eyewash Stations & Gene Transfer Studies: NIH Guidelines Explained
Blog Posts
How Long Should Eyes Be Flushed After Exposure?
Blog Posts
What Is the Accelerated Approval Pathway? Understanding the Latest FDA Guidance
Blog Posts
How Do PIs Report PRI in a Blinded Study Without Unblinding Themselves?
Blog Posts
Answering FAQs on HIPAA & PHI: Protect Participants’ Privacy & Ensure Compliance
Blog Posts
Does my clinic need to have an Exposure Control Plan in place?
Blog Posts
What Is Exempt Research?
Blog Posts
Ask the Experts: What Is E-consent? What Are E-signatures?
Blog Posts
Ask the Experts: What is the difference between a Risk Group and a Biosafety Level?
Blog Posts