Research and Clinical Trials
Use the Investigator's Guide for assist researchers in complying with Baptist Health System policies & Federal regulatio...
Read the questions about when to get Human Research Review Board approval for Clinical Trials at Shelby Baptist Medica...
Find information and procedures on the human subjects research projects conducted at the Baptist Health System
What Level of Review Do I Need?
Find details about qualifications for Exempt Research, Expedited Research and Full Committee Research for Clinical Trial...
Special Research Concerns
Find information for Special Concern including Emergency Use, children as subjects, pregnant women and other topics
Preparing and Submitting the Protocol and Consent
Get details on Preparing and Submitting the Protocol and Consent Document for Research and Clinical Trials
Managing the Project
Get information on managing Research and Clinical Trial programs including protocol, consent and review information
IRB Information and Fee Schedule
Get the Research and Clinial Trial Requirements and Checklist for Final Reporting Upon Study Completion
Get the Submission Instruction for New Clinical Trial submissions which need review by Full Human Research Review Board
Get the checklist for your application before you submit your human subjects protocol to the Human Research Review Board
Get the Research and Clinical Trial Consent Form Preparation checklist for studies at Shelby Baptist Medical Center
Get Research and Clinical Trial forms including Amendment, Continuing Review, Emergency Use Form & Informed Consent