Insights Archive

Drafting a Research Plan for IRB Review and Research Conduct: Information that Must Be Included in a Clinical Trial Protocol

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Adults with Limited Capacity to Consent to Research

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What are the requirements for notifications of study closure at research sites?

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Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans

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Managing the Shortage of Contrast Agents in Clinical Research Studies

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Do all subjects need to be reconsented with the revised consent form?

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Can a protocol get IRB approval during the 30-day IND waiting period?

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The Michael J. Fox Foundation Selects WCG as Institutional Review Board of Record for their Parkinson’s Progression Markers Initiative

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Does my customer survey project require IRB review?

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

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