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MGH Division of Clinical Research

IRB: New Submission

IRB Roundtable: New Submissions Speakers: Sheldon Ratnofsky, Human Research Specialist Learn how the Administrative Chairs (voting members of the IRB) review and consider ethical, scientific and regulatory aspects of human subjects research during full board review of new protocols. The …

MGH Division of Clinical Research

IRB Roundtable: Continuing Review and Amendments

Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI). Speakers: Jo O'Driscoll-Davis, Assistant Director for Continuing Review and Administrative Chair Michael Ducey, Senior Human Resource Specialist …

MGH Division of Clinical Research

IRB Roundtable: Amendments and Reporting to the IRB

Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI). Speaker:Jo O'Driscoll-Davis, Assistant Director for Continuing Review and Administrative Chair Per Federal Regulations, and Partners HRC policies, …

MGH Division of Clinical Research

IRB Roundtable: Consent Form Writing

Did you know that most of your research subjects are reading at the 8th-grade level or lower? Learn how to write the simplest, clearest consent forms, so that every one of your subjects can be fully informed. This workshop will …

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MGH Division of Clinical Research

IRB Issues for the Bench and Desk Scientist

Sponsored by the MGH Division of Clinical Research and the Human Research Committee Elizabeth Hohmann, MD, Chair and Physician Director, Partners Human Research Committee The purpose of this seminar is to discuss ethical, regulatory, and institutional issues relevant to analysis …

MGH Division of Clinical Research

Trial Innovation Unit Workshop: Resources for translating a great idea into the clinic

Sponsored by the Division of Clinical Research Speaker: Dr. Judy Hung Do you have a great idea but don’t know how to get it translated into clinical space? Join us for this workshop with Dr. Judy Hung, Director of Trial …

MGH Division of Clinical Research

What Does the IRB Really Want? How to Write a Human Studies Protocol

Sponsored by the MGH Division of Clinical Research and the Human Research Committee Elizabeth Hohmann, M.D., Chair and Physician Director, Partners Human Research Committee This practical lecture addresses "Full Review Protocols" - those of more than minimal risk which must …

MGH Division of Clinical Research

eIRB Training: A Hands-On Introduction to eIRB

This training is a hands-on workshop for users that need to submit to the Partners IRB. The workshop will focus on the basics of how to navigate, track, and submit common submission types using eIRB. The eIRB/Humans module within the …