Submit a New Study
New England IRB accepts study and site submissions via upload to FastTrack™ , email, fax or overnight courier. When sending any signed documents via FastTrack™ or email, please scan and send in PDF format.
The following materials may be required for review of your study:
Initial Protocol Submission
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New England IRB Protocol Submission Form
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Research Protocol
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Investigator's Brochure or Device Specifications, if applicable
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Proposed consent document (please use Microsoft Word format; send via email or include disc)
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Proposed patient information (instructions, surveys, diaries, etc.)
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Other supporting material (sample of any proposed advertising, etc.)
Investigator Instructions
When the study protocol has been submitted to New England IRB, please send site application materials below. If the protocol has not yet been submitted, please submit one set of the documents above in addition to the following:
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New England IRB Site Submission Form, signed by the principal investigator
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Current Curriculum Vitae of principal investigator(s)
(should include current practice address)
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Copy of current medical / nursing license for principal investigator
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Other supporting material (sample of any proposed advertising, etc.)
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Massachusetts investigators only: Copy of Researcher Registration
If you have any questions about the submission process, please call New England IRB, 617-243-3924 or e-mail New England IRB.
