Who can submit studies? Training Requirements Funding* Understanding HIPAA Guidelines for Submitting New Studies Specialized Topics - Decreased Decisional Ability - Guidelines for HUD Submission - IND Exemption Forms for Investigators - Legally Authorized Representatives - NCI CIRB Guidance for Submitting to the MCW/FH IRB
*MCW network access required
Continuing Progress Reports Guidelines Approved Protocol Changes Guidelines Unanticipated Events Guidelines* Protocol Deviations Guidelines*
Forms & Templates
New Consent Form Templates eBridge Quality Improvement Regulations & Guidance New & Draft Policies & Procedures
Studies that may meet criteria for Expedited Review
Studies that may be classified as Exempt from IRB Review
Consent Process Policies & Guidelines Forms & Templates Consultation & Audit Services Research Team Toolbox*
Committee Schedules & Membership Lists Committee Members Forms & Checklist
Resources for Patients & Research Subjects
NIH Senior Health Site
Becoming a Research Volunteer - English
Becoming a Research Volunteer - Spanish