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ANNEX 8Informed consent Form (ADAPTED FROM WHOGUIDELINE)Notes to Researchers:1. This informed consent contents different sections. Please chose the section which is relevant to your study2. Language
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How to fill out this informed consent contents

01
Start by reading the informed consent contents thoroughly to understand its purpose and what it entails.
02
Take note of any specific instructions or guidelines provided in the document.
03
Fill out your personal information accurately and completely, including your full name, date of birth, address, and contact details.
04
If applicable, provide additional information such as your medical history, current medications, or any known allergies.
05
Make sure to read and understand each section of the informed consent carefully.
06
If there are checkboxes or options to select, mark them according to your preferences or choices.
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If there are any areas that require your signature, ensure that you sign using your legal signature.
08
Date the document to indicate when you filled it out.
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10
If necessary, ask any questions or seek clarification from the relevant authority or person in charge.
11
Keep a copy of the filled out informed consent for your records.

Who needs this informed consent contents?

01
Anyone who is participating in a research study, clinical trial, medical procedure, or treatment that requires informed consent.
02
Patients seeking medical care or treatment where legal and ethical guidelines mandate the use of informed consent.
03
Individuals involved in activities or programs that involve potential risks, such as sports, recreational activities, or experimental therapies.
04
Parents or legal guardians of minors who are required to provide informed consent on behalf of the child or dependent.

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Informed consent contents include a detailed description of the study's purpose, procedures, potential risks, benefits, confidentiality measures, and the rights of the participants.
Researchers conducting studies involving human subjects are required to file this informed consent contents.
To fill out the informed consent contents, researchers should ensure all relevant information is clearly presented, written in understandable language, and includes signature lines for participants.
The purpose of informed consent contents is to ensure that participants are fully aware of what their participation involves, allowing them to make an educated decision about their involvement.
Information that must be reported includes study objectives, procedures, risks, benefits, confidentiality, and the voluntary nature of participation.
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