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Assessing Potential Risks in the Consideration of IND Exemption Criteria

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Defining “Minimal Risk” in Clinical Research

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WCG IRB Connecus Dashboard

WCG IRB Connexus Update: Version 5.5

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DNA strand

Highlighting the Growing Importance of Institutional Biosafety Committees in Clinical Research

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Managing the Shortage of Contrast Agents in Clinical Research Studies

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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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guidance documentation

Key Takeaways From FDA’s New Draft Guidance, “Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial”

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Compensating Research Participants FAQ

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Genetic Engineering And Gene Manipulation Concept

Four Key Elements You Need to Know About the Role of IBCs in Gene Therapy Trials

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