Resources

• 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.
  
  
• Dignity Health Guidelines for Writing a Minimal Risk Protocol
  These guidelines will help you provide information sufficient for an IRB determination.
  
  
• 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.

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