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Emory IRB Guidelines for Databases, Registries, and Specimen Repositories or repository protocol (and consent, if applicable), which may be very broad. document should be the basis for a meaningful exchange between the investigator and the subject.” FDA IRB Information Sheets –“A Guide to Informed Consent For the IRB current guidance for informed consent documentation and process, including the use of family members and research staff as interpreters, please go Does My Project Need IRB Review? Revised Common Rule at Emory · Study Submission Guidance · Consent Toolkit · Waivers · Certificates of Confidentiality Emory Informed Consent Form and Process Guidance Interpreters during Research Procedures, Including Consent Process, in Research conducted at Emory General guidance on submitting a new study can be found in the presentation, "10 Protocol Guidelines - for use in investigator-initiated studies and HUDs. A short form consent is used to enroll non-English speaking subjects when a version The procedure for using a shortform is described in the IRB Policies and Emory IRB Guidance for Investigators. Version 3-2-17. Emory Guidance for the use of Electronic Informed Consent. Background. The purpose of this document isProtocol & Lay Summary format can be found under “New Study. Guidance: www.irb.emory.edu/forms/new.html. ? Consent templates and consent-related If you are a new investigator at Emory, please review this guidance. In addition, you can make an appointment with the IRB to take stock of your studies and