IRB regulations provide a variety of tools for effective implementation of the informed consent process. What are these tools, what flexibility is available for investigators so that the rights of research participants’ are respected while research moves forward in achieve its scientific objectives? Specific guidance will be provided for applying these regulatory flexibilities appropriately.
The seminar will be held in the Research Affairs main conference room from 12-1pm. Physicians attending this session will earn CME.
You must register to receive credit and so we can have lunch ready for you. Seating is limited.
Please click link Register
Thank you for your attention. We look forward to seeing you there.
