Covid-19 Insights

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WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic

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The Basics of the Individual Expanded Access Request Process: A Resource for Physicians

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Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment

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How do EUAs for COVID-19 vaccines affect IBC oversight requirements for ongoing clinical trials?

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[Webinar] IRB and IBC Required Approvals in Gene Therapy: Addressing Challenges in a Growing Market

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WCG IRB’s Response to COVID-19 in 2020: Supporting the Clinical Trial Industry When It Needed It the Most

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Should we exclude subjects who recently received COVID-19 vaccine from participating in other research studies?

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Is IRB review required to collect specimens for a new test to diagnose COVID-19?

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Informed Consent and COVID-19: An IRB Perspective on Navigating the New Normal

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How Should I Handle Changes to Research Made in Response to COVID-19?

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