Saint Louis University

Investigator Resources

 

Getting Started: IRB Process at a Glance

General Guidelines for Conducting Research at SLU 

Tips for Choosing the Appropriate IRB Application

 

Investigator Initiated Clinical Research:

  • CITI Good Clinical Practice (GCP) Training: 

Clinical researchers are encouraged to take this optional GCP Course to learn more about regulations that are unique to clinical trials and the importance of using good clinical practice in the conduct of clinical research. See the Training and Education page for more information about registering for CITI training.

 

Checklists and Decision Trees:

Additional Criteria Checklist: Department of Defense 

Additional Criteria Checklist: Department of Education 

Additional Criteria Checklist: Department of Energy

Additional Criteria Checklist: Department of Energy - PI Checklist

Additional Criteria Checklist: Department of Justice

Additional Criteria Checklist: Environmental Protection Agency

Additional Criteria Checklist: Investigational Devices

Additional Criteria Checklist: Investigational Drugs

Additional Criteria Checklist: Sponsor Investigator Responsibilities

Checklist: Human Research Determination

Checklist: Eligibility for Exempt Review

Checklist: Eligibility for Expedited Initial Review

Checklist: Eligibility for Expedited Continuing Review

Checklist: Obtaining Consent in 45 CFR 46.406/21 CFR 50.53 Research

Decision Tree: Protocol Violation

Decision Tree: Serious Adverse Event

Decision Tree: Unanticipated Problem

 

Higher purpose. Greater good.
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