JHM IRB Consent Language Requirements for Department of Defense (DoD)-Funded Research
December 2020
The information provided in this document is for DoD-sponsored studies.
For all participants in DoD-funded research, the informed consent documents must include the following:
Section of the Consent |
What is Required? |
Sponsor/Supporter/Funded By: (located on p. 1 of the written and oral consent templates; see links to templates on last page below) |
|
What treatment costs will be paid if you are injured in this study? |
|
How will your privacy be maintained and how will the confidentiality of your data be protected? |
|
IN ADDITION:
For participants who are DoD-affiliated personnel, the informed consent documents must include the following if implicated:
Section of the Consent |
What is Required? |
What are the risks or discomforts of the study? |
If you have questions about whether these issues may be implicated for your study, you should consult with your funding source/the DoD’s Human Research Protection Official (HRPO). |
JHM IRB Written Consent Template: https://www.hopkinsmedicine.org/institutional_review_board/forms/JHMIRB_CombinedInformedConsent_Template_v17.docx
JHM IRB Oral Consent Template: https://www.hopkinsmedicine.org/institutional_review_board/forms/OralConsentScript.docx