Learning Objectives:

1.  To understand and appreciate the background and ethical principles that have led to the development of the IRB process

2.  To understand the foundations and importance of informed consent and the role of the federal regulations and the IRB in shaping this process

3.  To understand the metrics related to "IRB review times" and the obligations of Physician Investigators in contributing to, and improving, these review times

Session date: 
06/28/2021 - 12:00pm to 1:00pm CDT
  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation

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Speaker Name: 
Christopher Daugherty, MD