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How to Name Documents for Submission to the IRB


The page outlines the nomenclature study teams are required to use when submitting documents to the NIH IRB.  Each electronic regulatory file must have a consistent format, including naming of folders and files, to ensure required information is maintained and easily accessible.  Per the International Council for Harmonisation Good Clinical Practice Guidelines, essential documents allow for evaluation of the conduct of the study and quality of the study data.



Things to Remember

Protocol Nomenclature

Consent Nomenclature

Other Study Documents



Things to Remember




Protocols




Consents


If conducted at the Clinical Center and the NIEHS CRU


If NOT conducted at the Clinical Center and the NIEHS CRU

***Please Note: For Assents change the word “Consent” to “Assent” in the filename.***



Examples of Nomenclature for Other Study Documents