Ask the IRB and 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 built this forum as an immediate and less formal way to share information across the clinical research community.
Submit your clinical trial ethical or regulatory question to our IRB and IBC experts
Most recent:
Answering FAQs on HIPAA & PHI: Protect Participants’ Privacy & Ensure Compliance
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Why do Community Members Need to Participate in IBC Review Meetings?
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If a site needs to submit to create an IBC with WCG, how long does the NIH registration process typically take?
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Does my clinic need to have an Exposure Control Plan in place?
Blog Posts What Is Exempt Research?
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What Is Expedited Review?
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Ask the Experts: What Is E-consent? What Are E-signatures?
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Ask the Experts: What is the difference between a Risk Group and a Biosafety Level?
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What Information Must Be Included in the Cost Section of an Informed Consent Form?
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What Is Assent, When Provided by an Adult Participant Lacking Capacity? And What Are WCG’s Expectations and the Investigator’s Responsibilities?
Blog PostsMeet the experts:
Our experts, with decades of experience and a deep knowledge of regulations, ethics, and research best practices, will answer anything related to research ethics and research oversight including institutional review board operations, practice and regulations. We post the questions (anonymized) and answers on our website, as a resource for our industry.
Submit your question here
Submit questions to us on anything related to research ethics and research oversight including institutional review board operations, practice and regulations. Our experts, with decades of experience and a deep knowledge of regulations, ethics, and research best practices, will answer. We’ll post the questions (anonymized) and answers on our website.
Before using this form, please note:
- Protocol-specific questions for studies under the oversight of a WCG IRB should be submitted through your IRB contact person, not through this form.
- If your question is about what needs to be promptly reported to the IRB during a study, please see form HRP-204 and this manual for guidance.
Disclaimer:
WCG may not be able to respond to all questions and cannot respond to any medical questions or provide referrals for clinical care or studies.
You acknowledge that any question submitted to this site may be publicly available and that your use of this site is subject to the WCG Terms of Use.