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.
Regulatory Compliance
Why do Community Members Need to Participate in IBC Review Meetings?
Blog Posts
Series: Ask the IRB & IBC Experts
If a site needs to submit to create an IBC with WCG, how long does the NIH registration process typically take?
Blog Posts
Series: Ask the IRB & IBC Experts
Does my clinic need to have an Exposure Control Plan in place?
Blog Posts
Ethics in Clinical Research
What Is Exempt Research?
Blog Posts
Ethics in Clinical Research
What Is Expedited Review?
Blog Posts
Ethics in Clinical Research
Ask the Experts: What Is E-consent? What Are E-signatures?
Blog Posts
Series: Ask the IRB & IBC Experts
Ask the Experts: What is the difference between a Risk Group and a Biosafety Level?
Blog Posts
Ethics in Clinical Research
What Information Must Be Included in the Cost Section of an Informed Consent Form?
Blog Posts
Ethics in Clinical Research
What Is Assent, When Provided by an Adult Participant Lacking Capacity? And What Are WCG’s Expectations and the Investigator’s Responsibilities?
Blog Posts
Ethics in Clinical Research