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ACRP 2019 OnDemand

157 - Integrating Quality into Investigator-Initiated Clinical Trials

Apr 13, 2019 10:15am ‐ Apr 13, 2019 11:15am

Credits: None available.

Non Member: $75.00
Members: $15.00


There are many steps that must be taken to assess risk and integrate quality when developing, initiating and conducting a clinical trial. These steps are crucial for every type of clinical trial. This session will describe how to apply those principles to investigator-initiated clinical trials utilizing tips, tools and templates available to help along the way.

Learning Objectives:

  • Identify quality standards, and areas of risk, for clinical trials.
  • Describe measures to incorporate quality into study design and initiation of Investigator-Initiated Trials (IITs).
  • Examine ways to assess quality during IIT study conduct.


  • Neala Lane, MS, CCRC, Associate Director, Quality Improvement Office, Indiana University

Credits Available

Integrating Quality into Investigator-Initiated Clinical Trials Exam

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Janice Prodell
5/5/19 3:09 pm

Can your slides and forms be shared? Great lecture, thank you!