Resources

We've provided you with a variety of resources for your convenience

• Basic & Additional Elements of Informed Consent
  
  • Informed Content - Key Elements
  • Guidance for Developing Informed Consent Documents
• Belmont Report
  This report attempts to summarize the basic ethical principles identified by the Commission in the course of its deliberations.
• Definitions
  Terms explained for Basic HHS Policy for Protection of Human Research Subjects.
• Federalwide Assurance
  An assurance of compliance with the HSS regulations for the protection of human subjects.
• Glossary of Terms
  Is a complied glossary of the most frequently used terms in clinical trials.
• Good Clinical Practice
  An international set of guidelines used as a standard.
• Important Links
  It is our hope these links will provide you with the best information.
• ORHP Policies & Guidance
  It is our hope that the OHRP Policies & Guidance will help you become more familiar with the regulations.
• Reviewer Toolkit
  This section contains reference materials and useful links for IRB members.

Should you require additional guidance, please call the East Valley Regional IRB at (480) 728-3582.