Med/Sci
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FDA & ICH
Does my customer survey project require IRB review?
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COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
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Protecting Patients, Protecting Your Study: The Benefits Of A Well-Run Data Monitoring Committee
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Cell & Gene Therapy
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
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Series: Ask the IRB & IBC Experts
Is informed consent needed for post-market patient registry?
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Diversity & Inclusion
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
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Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
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Should You Be Adjudicating Your Clinical Endpoints?
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Clinical Endpoints
NASH Knowledge Forum: Evolving Industry Best Practices and Trends for Endpoint Adjudication and Imaging in NASH Trials
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Clinical Endpoints