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This document serves as an authorization form allowing the disclosure and use of health information for research purposes by William Beaumont Army Medical Center and associated personnel.
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How to fill out sample hipaa research authorization

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How to fill out SAMPLE HIPAA RESEARCH AUTHORIZATION

01
Title the document as 'HIPAA Research Authorization'.
02
Include your name and contact information at the top.
03
Specify the purpose of the authorization, clarifying it is for research purposes.
04
Clearly outline the information being authorized for use, such as health records and personal data.
05
Identify who will use the information, stating the research team and any affiliated organizations.
06
State any potential risks or benefits to the participant regarding the use of their information.
07
Include options for the participant to revoke the authorization and describe how to do so.
08
Provide a space for the participant’s signature and date, along with a witness signature if required.

Who needs SAMPLE HIPAA RESEARCH AUTHORIZATION?

01
Researchers conducting studies that require access to protected health information.
02
Healthcare providers who need to collect and use health data for research purposes.
03
Institutions involved in medical research that mandates compliance with HIPAA regulations.
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People Also Ask about

An authorization is a HIPAA required document that defines only the terms and conditions of permission to use or disclose specified PHI for a specified research project.
I hereby authorize use or disclosure of protected health information about me as described below. 4. ​ I understand that the information used or disclosed may be subject to re-disclosure by the person or class of persons or facility receiving it, and would then no longer be protected by federal privacy regulations.
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.
An authorization document must include all of the following: Description of information to be use or disclose, identification of person authorized to use or disclose information, name of person(s) or group to whom PHI may be given, purpose of use or disclosure, expiration date, valid signature and date.
Answer: Under the HIPAA Privacy Rule you must meet certain requirements before using or disclosing individually identifiable health information for research. (These HIPAA requirements are in addition to IRB requirements under federal regulations for the protection of human subjects.)
The name(s) or other specific identification of the person or class of persons to whom information will be disclosed. A description of the purpose of the requested use or disclosure. In cases where a statement of the purpose is not provided, “at the request of the individual” is sufficient.

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SAMPLE HIPAA RESEARCH AUTHORIZATION is a document that allows researchers to obtain and use protected health information (PHI) for research purposes in compliance with the Health Insurance Portability and Accountability Act (HIPAA) regulations.
Researchers and institutions conducting studies that involve the use of PHI must obtain and file SAMPLE HIPAA RESEARCH AUTHORIZATION from participants before accessing their health information.
To fill out SAMPLE HIPAA RESEARCH AUTHORIZATION, the researcher must include the study's purpose, detailed information about the PHI to be used, any potential risks, the duration of the authorization, and ensure that the participant's signature and date are present.
The purpose of SAMPLE HIPAA RESEARCH AUTHORIZATION is to protect individuals' privacy while allowing researchers to legally access and utilize their health information for scientific and clinical investigations.
The SAMPLE HIPAA RESEARCH AUTHORIZATION must report information such as the purpose of the research, details regarding the types of PHI being collected, how the information will be used, any potential risks to the participant, and the effective dates of the authorization.
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