Preparing the Human Subjects Study Record

Applications for research funding that involves human subjects require comprehensive documentation of the investigator’s plans to collect information, perform research activities and protect subjects. In addition to obtaining internal approvals via MSU’s Institutional Review Board, the proposal may require a “Human Subjects Study Record” in which specific details must be provided on the subjects and study itself, plans for mitigating any risks, and potential benefits of the proposed study, among others.

This virtual seminar will provide instructions (including templates and forms) on completing both the internal IRB approval process via MyProtocol and the required PHS Human Subjects Study Record form and associated attachments, as well as how to include them with a proposal during submission.

Register for free