IRB Policies and Procedures

To request previous versions of any of the IRB policies listed below, please call the IRB Office at (321) 841-5895 

IRB Structure

• Ethical Principles 0330-1017
• IRB Membership and Structure 0330-1013
• IRB Authority and Jurisdiction 0330-1005
• Use of a Single IRB of Record 0330-1023

Types Of IRB Review

• Compassionate Use/Treatment Use/Expanded Access of Investigational Drug or Device 0330-1012
• Emergency Use of Investigational Drugs and Devices 0330-1010
• Exempt Review 0330-1004
• Expedited Review 0330-1003
• HIPAA Research and Privacy Board Policy 0330-1024
• HUD Policy 0330-1006
• Use of External IRB of Record 0330-1025

IRB processes

• Advertising, Recruiting and Media Contact for Research Subjects 0330-1021
• Amendment Review Process 0330-1008
• Continuing Review Process 0330-1007
• IRB Definition Policy 0330-1026
• Informed Consent Process 0330-1002
• IRB Process for Receiving Complaints 0330-1009
• New Protocol Submission 0330-1014
• Protocol Deviations/Violations/Non-compliance 0330-1001
• Reporting Serious Adverse Events 0330-1000
• Study Closure, Termination or Suspension of Research 0330-1019
• Translation of Study Documents 0330-1022

Vulnerable Population

• Children in Research Including Unmarried Pregnant Minors, Unmarried Minor Mothers, Married Minors, and Emancipated Minors 0330-1011
• Research Involving Pregnant Women, Fetuses and Neonates 0330-1016
• Research Involving Prisoners 0330-1020
• Research On Decedents 0330-1018