How do you determine whether your IRB is meeting all applicable regulatory requirements and ethical standards? National experts in human subject protection will share best practices and discuss how and why they do what they do to mitigate the risks of human research. Presentations will cover such items as protocol review, investigator training, post-approval monitoring, and how operations/compliance/audit offices can work together to mitigate the risks. Ample time will be allotted for questions and discussion. |
