IRBs are in a unique position to impact risk management in clinical research. Their role is designed to protect research participants, but this can also equate to elevating best practices in risk management and enabling higher quality studies. Their role is designed to help reduce risk to research participants, but this role enables valuable insight into trial risk management and quality management systems. This session will explore how sponsors and CROs can leverage the IRB in light of its purpose and visibility into data and systems to improve risk management in the clinical research enterprise.
We will discuss real-world examples of how IRBs can further improve risk management and quality systems through education, expanded feedback, and information coordination from all aspects of a clinical trial.
Mitchell E. Parrish
JD, RAC, CIP
Content applies to sponsors, CROs, and IRB members.
The presentation may qualify for continuing education credits; check with your certifying organization(s) for more information.
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