Info Sheet

IRB Review Services for Phase I Research

Our dedicated team and processes are built to support your Phase I research needs.

Rely on customized IRB capabilities to ensure appropriate, efficient reviews:

  • Responsive, multi-functional team to ensure service excellence and eliminate delays
  • Real-time access to review status information and approval documents
  • Daily specialized IRB panels to review Phase I research and changes to previously approved research
  • IRB review and approval issued prior to FDA 30-day investigational new drug (IND) wait period

To learn more, fill out the form to download the info sheet.





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DATE
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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