This page is meant to provide investigators with some tools to assist them with their research. These are not forms that need to be submitted to the IRB. Please feel free to modify the forms to fit your needs.

	Documenting the informed consent process	Medical Record Note Research Record Note
	Keeping track of your submissions to the IRB	Submission Tracking Log
	Keeping track of adverse events	Adverse Event Tracking Log
	How to set up a regulatory binder	Regulatory Binder Template
	Keeping track of research related duties that have been delegated by the PI to others (note: the PI is still responsible)	Delegated Duties Log
	Enrolling Children in Research	Worksheet for involving Children Signature Criteria for Minor Subjects (children) Kids to Adults: reconsenting flow chart Kids to Adults: reconsenting FAQ Kids to Adults: special Informed Consent form for follow-up
	How to identify and recruit research subjects	Identifying & Recruiting Research Subjects