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Institutional Review Board (IRB) Forms
Form NameDownloads
IRB Application Form(Word) (PDF)
Change in Investigator Form(Word) (PDF)
Continuing Review or Closure Form of Therapeutic Research (Word) (PDF)
Informed Consent Form (Word) (PDF)
Waiver of Consent Form (Word) (PDF)
Serious Adverse Event(Word) (PDF)
Survey Consent Form (Word) (PDF)
HIPAA Form (Word) (PDF)
HIPAA Waiver Form (Word) (PDF)
IRB Application Form(Word) (PDF)
Protocol Deviation Report (Word) (PDF)
Protocol Violation Report (Word) (PDF)
Addendum and Revision Form (Word) (PDF)
Child Assent Form (Word) (PDF)
Child Assent Example Form(Word) (PDF)
Conflict of Interest Policy(Word) (PDF)
Conflict of Interest Signature Form(Word) (PDF)
Exempt Policy(Word) (PDF)
Exempt Form(Word) (PDF)
The IRB is guided by the ethical principles regarding all research involving humans as subjects as set forth in the report of the National Commission of the Protection of Human Subjects of Biomedical and Behavioral research entitled Ethical Principles and Guidelines for the Protection of Human Subjects of Research The Belmont Report. The IRB is guided by principals set forth by the Ascension Ethical and Religious Guidelines. Ethical considerations are also set forth in The Declaration of Helsinki.

Other AttachmentsDownloads
1. Ascension Ethical and Religious Guidelines (Word) (PDF)
2. The Belmont Report (Word) (PDF)
3. Declaration of Helsinki (Word) (PDF)
4.The Nuremberg Code (Word) (PDF)
5. Standard Operation Policies(Word) (PDF)

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