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Get the free Authorization for Use and Disclosure of Protected Health Information in Research - nova

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This document serves as authorization for researchers to access and use personal health information for a study conducted by Nova Southeastern University, outlining the rights of the participant regarding
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How to fill out Authorization for Use and Disclosure of Protected Health Information in Research

01
Obtain the Authorization for Use and Disclosure of Protected Health Information form.
02
Read the instructions carefully to understand the requirements.
03
Fill in the participant's name, contact information, and date of birth.
04
Specify the purpose of using the protected health information (PHI) for research.
05
Describe the types of PHI that will be collected and used in the research.
06
Indicate the researchers and institutions that will have access to the PHI.
07
Specify the duration for which the authorization is valid.
08
Include a statement about the participant's right to revoke the authorization at any time.
09
Provide space for the participant's signature and date.
10
Offer a copy of the signed authorization to the participant.

Who needs Authorization for Use and Disclosure of Protected Health Information in Research?

01
Researchers conducting studies that involve accessing or using protected health information.
02
Institutions or organizations involved in the research that require PHI.
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People Also Ask about

Short Answer: Individuals generally must authorize any use or disclosure of their PHI that is not for treatment, payment, or health care operations. HIPAA authorizations must contain specific “core elements” and required statements to be valid.
Answer: Informed consent is required under federal research regulations for the protection of human subjects. The HIPAA Privacy rule, a different regulation, separately requires that patients give written Authorization before a covered entity may use or disclose patients' protected health information for research.
Under the HIPAA Privacy Rule, covered entities may use or disclose protected health information from existing databases or repositories for research purposes either with individual authorization as required at 45 CFR 164.508, or with a waiver of individual authorization as permitted at 45 CFR 164.512(i).
Although it is in most cases preferable to get permission to use an individual's Protected Health Information, HIPAA permits research using PHI without obtaining consent (called Authorization by HIPAA).
I understand that I have the right to inspect or have a copy of the confidential information I have authorized to be used or disclosed by this authorization form. I understand that if I agree to sign this authorization, which I am not required to do, I must be provided with a signed copy of the form.
All authorizations must be in plain language, and contain specific information regarding the information to be disclosed or used, the person(s) disclosing and receiving the information, expiration, right to revoke in writing, and other data.
A Privacy Rule Authorization is an individual's signed permission to allow a covered entity to use or disclose the individual's protected health information (PHI) that is described in the Authorization for the purpose(s) and to the recipient(s) stated in the Authorization.
An IRB can grant a Waiver of HIPAA Authorization to permit use and/or disclosure of PHI for research purposes, without obtaining authorization. An IRB may also approve an alteration of the requirements of written HIPAA Authorization provided the research meets the criteria for waiver or alteration (see info below).

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Authorization for Use and Disclosure of Protected Health Information in Research is a formal agreement that allows researchers to use and share a participant's private health information for research purposes while ensuring confidentiality and compliance with privacy laws.
Researchers conducting studies that involve accessing or utilizing protected health information (PHI) from individuals must file the Authorization. This typically includes institutions, hospitals, and any researchers who handle PHI.
To fill out the Authorization, the researcher must complete a form that includes the participant's identification details, descriptions of the information being collected, the purposes of the research, and any potential risks. Additionally, participants must provide their signature and date to indicate consent.
The purpose of the Authorization is to protect participants' privacy by ensuring they have control over their health information while allowing researchers to access necessary data for legitimate research purposes.
The information that must be reported includes the participant's name and contact information, a description of the protected health information being used, the purpose of the research, the entities that may use the information, and the expiration date of the authorization.
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