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Accessibility Statement

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We are working to have the website conform to the relevant standards of the Section 508 Web Accessibility Standards developed by the United States Access Board, as well as the World Wide Web Consortium's (W3C) Web Content Accessibility Guidelines 2.1. These standards and guidelines explain how to make web content more accessible for people with disabilities. We believe that conformance with these standards and guidelines will help make the website more user friendly for all people.

Our efforts are ongoing. While we strive to have the website adhere to these guidelines and standards, it is not always possible to do so in all areas of the website. If, at any time, you have specific questions or concerns about the accessibility of any particular webpage, please contact WebsiteAccess@tenethealth.com so that we may be of assistance.

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  1. Research and Clinical Trials
  1. Health Professionals
  2. Research and Clinical Trials
  3. Forms

Forms

BBH IRB forms have been revised as of September 2016. New versions of these forms will be required for all submissions received after October 10, 2016.

  • New Application
  • FDA-1572
  • Instructions for filling out Form FDA 1572
  • Expedited Review Application
  • Informed Consent "Template"
  • Waiver of Informed Consent "form"
  • Amendment Application
  • Continuing Review Application
  • Termination Application
  • Emergency Use Form
  • Surrogate Consent "form"  
  • Adverse Event Inside BBH
  • Adverse Event Outside BBH

Research and Clinical Trails Resource

Introduction
FAQs
Getting Started
What Level of Review Do I Need?
Special Research Concerns
Preparing and Submitting the Protocol and Consent
Managing the Project
IRB Information and Fee Schedule
Appendix I
Appendix II
Appendix III
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