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Northwestern University Consent Form and HIPAA Authorization for Research 2014-2025 free printable template

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Version Date: 10/23/2014Northwestern University (Department of Radiology)Consent Form and HIPAA Authorization for Research Patient Consent PROTOCOL TITLE: Dualvenc 4D Flow MRI of Unruptured Intracranial
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How to fill out Northwestern University Consent Form and HIPAA

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How to fill out Northwestern University Consent Form and HIPAA Authorization

01
Obtain the Northwestern University Consent Form and HIPAA Authorization documents from the appropriate source.
02
Read through the instructions carefully to understand the information required.
03
Fill out personal information, including your name, date of birth, and contact information.
04
Provide details about the study or treatment you are consenting to, including the purpose and any risks involved.
05
Sign and date the consent form where indicated to confirm your agreement.
06
If applicable, include names of any other individuals authorized to access your health information under HIPAA.
07
Review the completed forms to ensure all information is accurate and complete.
08
Submit the forms to the designated department or individual as instructed.

Who needs Northwestern University Consent Form and HIPAA Authorization?

01
Individuals participating in research studies at Northwestern University.
02
Patients receiving treatment that involves sharing their health information.
03
Anyone whose health information will be accessed by researchers at Northwestern University.
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The Northwestern University Consent Form and HIPAA Authorization is a document that allows individuals to give permission for their health information to be used and disclosed for research or other purposes in accordance with privacy regulations.
Participants in research studies or programs at Northwestern University that involve the use of personal health information are required to file the Consent Form and HIPAA Authorization.
To fill out the form, individuals must provide personal information, indicate their agreement to participate in the study, and authorize the use of their health information as specified. Guidance is usually provided by the research team.
The purpose is to ensure that participants are fully informed about the research study and the use of their health information, and to obtain legal permission for this information to be shared.
The form must include personal identification details, information about the research study, details about health information usage, and the participant's signature indicating consent.
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