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UNIVERSITY HOSPITALS CLEVELAND MEDICAL CENTER IRB NUMBER: 099930. IRB APPROVAL DATE: 9/24/2019 IRB EFFECTIVE DATE: 9/25/2019 IRB EXPIRATION DATE: 7/8/2020CONSENT FOR INVESTIGATIONAL STUDIES (v.09.2016)
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01
Start by opening the LTBI Test Consent Document (LTBITestConsentDocument.doc).
02
Fill in the patient's name, date of birth, and contact information in the designated fields.
03
Provide information about the healthcare provider who will be administering the LTBI test, including their name, contact information, and any relevant credentials.
04
Read and understand the provided information about the LTBI test, its purpose, potential risks, and benefits.
05
If applicable, indicate any allergies or medical conditions that may affect the LTBI test or the patient's ability to undergo the test.
06
Review and consent to any required disclosures and authorizations related to the LTBI test.
07
Sign and date the consent document in the provided spaces.
08
Keep a copy of the filled-out LTBI Test Consent Document for your records.
09
Submit the completed LTBI Test Consent Document to the healthcare provider conducting the LTBI test.

Who needs ltbitestconsentdocumentdoc?

01
Anyone who is scheduled to undergo the LTBI test, which is used for detecting latent tuberculosis infection (LTBI), needs the LTBI Test Consent Document (LTBITestConsentDocument.doc). This document ensures that patients have provided their informed consent for the test and have understood its purpose, potential risks, and benefits. Healthcare providers require this consent document to comply with legal and ethical obligations in obtaining informed consent from their patients.
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ltbitestconsentdocumentdoc is a test consent document for an experimental treatment.
The individual participating in the experimental treatment is required to file ltbitestconsentdocumentdoc.
ltbitestconsentdocumentdoc should be filled out by providing consent for the experimental treatment and acknowledging any potential risks.
The purpose of ltbitestconsentdocumentdoc is to ensure that individuals are fully informed and give their consent for participating in experimental treatments.
ltbitestconsentdocumentdoc must include details of the experimental treatment, potential risks, and the individual's consent acknowledgment.
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