Events

This session will provide:

- A history of human subjects protection and the ethical principles that guide human subjects research;

- An overview of the federal regulations for the protection of human subjects in research;

- Criteria for IRB review;

- Tips for submitting complete and understandable new protocols, modifications, renewals and adverse event reports;

- Tips for obtaining IRB approval more quickly;

- The RASCAL system;

- The IRB review process.

Who should attend?

- Research personnel who have not attended the IRB 101 series in the past;

- Individuals new to the research environment;

- Research personnel new to Columbia;

- All those who wish to gain a historical perspective and learn the ethical and regulatory guidelines for Human Subjects Research.

Beverages and a light lunch will be provided.