eBridge
IRB Standard Procedures and MCW Research Policies
Consent Form Templates
IRB Forms & Templates
Training Requirements
Understanding HIPAA
Safety Committees*
Audits and Routine Reviews
IRB Committee Rosters
Federalwide Assurance
Federal Regulations
MCW Office of Research*
Human Stem Cell Research Oversight Committee
Funding
This page provides access to information that will be helpful as you start a new study submission. Here the IRB answers questions about who can submit new studies, provides links to OHRP decision charts, and more.
This page provides access to procedures that will be helpful if you need to change your original study submission. This can occur when study staff changes, study procedures change, when a change is need in a consent form, etc. Here you will also find a link for the procedure for submission of amendments.
This page provides access to information that will be helpful to you when you need to report a protocol deviation or have an unanticipated event.
***This section is currently under construction.***
This page provides access to procedures that will be helpful to you when you are submitting a Continuing Progress Report in eBridge for your study.