Irb Review Insights

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

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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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Using an IRB’s Site Relationships to Relieve “Site Crunch” and Reduce Trial Pressures

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WCG IRB Site Partnerships

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

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The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation

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