IntegReview: Committed to the Protection of Research Subjects IntegReview: Committed to the Protection of Research Subjects  
The Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) Integreview
 
 

IntegReview
IntegReview Ethical Review Board
3001 S. Lamar Blvd., Suite 210
Austin, TX 78704
Phone: 512-326-3001
Fax: 512-697-0085
Email: integreview@integreview.com
 

Research Subject Bill of Rights

As a subject involved in an investigational research study, you have the following rights:

  1. Be informed of the nature and purpose of the experiment.
  2. Be given an explanation of the procedures to be followed in the medical experiment, and any drug or device to be used.
  3. Be given a description of any attendant discomforts and risk reasonably to be expressed from the experiment.
  4. Be given an explanation of any benefits to the subject reasonably to be expected from the experiment, if applicable.
  5. Be given a disclosure of any appropriate alternative procedures, drugs, or devices that might be advantageous to the subject, and their relative risks and benefits.
  6. Be informed of the avenues of medical treatment, if any, available to the subject after the experiment if complications should arise.
  7. Be given an opportunity to ask any questions concerning the experiment or the procedures involved.
  8. Be instructed that consent to participate in the medical experiment may be withdrawn at any time. The subject may discontinue participation in the medical experiment without prejudice.
  9. Be given a copy of a signed and dated written consent form when one is required.
  10. Be given the opportunity to decide to consent or not to consent to a medical experiment without the intervention of any element of force, fraud, deceit, duress, coercion, or undue influence on the subject’s decision.
 
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