This handout information should be placed in a binder which will help organize your study and be a source that provides a complete and thorough history of your research study from protocol development to study completion.  The binder should include all versions of the study protocol, your standard operating procedures (SOP), Informed consent documents, recruitment materials, surveys/ questionnaire/ other instruments of your research study and correspondence between the IRB, sponsor and other regulatory bodies as applicable.  The purpose of this binder is to store and organize required study documents and correspondence. 

Section A: Regulatory Binder Binder

Section B:  Drug Device Binder Tabs

Section C:  GCP Guidance Information

Participant identifiable documents such as signed informed consents should be maintained separately in a subject specific binder/file.

Please contact Jacqui Poore at 401-444-5843 or if you have questions or require assistance.