Training Calendar

This course will take the student through the step-by-step process of obtaining subject informed consent.

This training will provide an introduction to human subjects research regulations; the differences between Exempt, Expedited, and Full Board reviews; and an introduction to human subject research involving vulnerable populations.

In this course, participants will learn the process for developing an effective Corrective and Preventive Action Plan (CAPA). It will cover when and why CAPAs are needed, ways to identify a root cause, and tools to facilitate the process.

This course will take the student through the step-by-step process of obtaining subject informed consent.

This training provides an introduction to secondary research, including how to prepare documents for COMIRB review. Time will be reserved to discuss your secondary research projects.

This course will take the student through the step-by-step process of obtaining subject informed consent.

This course will provide an overview of the ClinicalTrials.gov system including the requirements for posting a trial, common mistakes when posting and continuing responsibilities.