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