Single IRB Review: Tips for Sponsors and CROs Working with Institutional Sites

Single IRB mandates help ensure significant resource savings and efficiencies for clinical trials. How do you ensure your sites are prepared to comply with FDA’s sIRB mandate?

This eBook provides a toolkit to:
  • Understand the institutional IRB’s role when sIRB review is utilized
  • Assess and update policies to comply with sIRB requirements
  • Leverage best practices to optimize sIRB efficiencies

Download the eBook to learn more.

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