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End Clinical Trial Research Adult Consent/Assent Form Version 4.3 Version Date: 05 Jul 2022___ SUBJECT IDENTIFICATIONProtocol Title: end (Evaluating Newly Approved Drugs in Combination Regimens for MultidrugResistant

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How to fill out 2a endtb-qresearch adult consentassent

01

Begin by explaining the purpose of the study and the information that will be collected.

02

Provide a clear explanation of the risks and benefits of participation.

03

Ensure that the participant understands that participation is voluntary and that they can withdraw at any time.

04

Obtain written consent from the participant or their legally authorized representative.

05

Document the consent process and provide a copy of the consent form to the participant.

Who needs 2a endtb-qresearch adult consentassent?

01

Any adult who is participating in the endtb-qresearch study requires 2a endtb-qresearch adult consent/assent.

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What is 2a endtb-qresearch adult consentassent?

2a endtb-qresearch adult consentassent is a form that allows an adult to give their consent or assent to participate in a research study or clinical trial.

Who is required to file 2a endtb-qresearch adult consentassent?

Adult participants who are involved in a research study or clinical trial are required to fill out and file 2a endtb-qresearch adult consentassent.

How to fill out 2a endtb-qresearch adult consentassent?

To fill out 2a endtb-qresearch adult consentassent, the adult participant needs to carefully read the information provided, sign the form to indicate their consent or assent, and provide any required personal information.

What is the purpose of 2a endtb-qresearch adult consentassent?

The purpose of 2a endtb-qresearch adult consentassent is to ensure that adult participants in a research study or clinical trial willingly consent to participate and understand the risks and benefits involved.

What information must be reported on 2a endtb-qresearch adult consentassent?

2a endtb-qresearch adult consentassent must include information about the research study or clinical trial, the risks and benefits involved, the participant's rights, and any required personal information.

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