Insights Archive

Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research

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Making Clinical Research Inclusive: Strategies to Include the LGBTQIA+ Community in Research Trials

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Can a physician submit a single humanitarian use device (HUD) submission to the IRB?

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Compensating Research Participants FAQ

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WCG IRB Welcomes 2021 Class to International Fellows Program on Research Ethics

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What questions can be asked when screening patients prior to them signing consent?

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When do I report a protocol deviation to the IRB? Do I need to report a summary of deviations at the time of continuing review?

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What documentation needs to be submitted to the IRB for an IND exemption request?

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[Video] Institutional Biosafety Committee Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials

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[Webinar] The Do’s and Don’ts of Compensating Research Participants: Guidance for Clinical Research Stakeholders

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