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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 informed consent form adapted

01
Gather all necessary information and documents required for the informed consent form.
02
Read the instructions and guidelines provided with the form.
03
Start filling out the form by providing personal information such as name, address, and contact details.
04
Specify the purpose and nature of the study or procedure that requires informed consent.
05
Include detailed information about the risks, benefits, and alternatives of participating in the study or procedure.
06
Clearly explain the voluntary nature of participation and the right to withdraw consent at any time.
07
Provide information about any compensation or incentives offered for participation, if applicable.
08
Include a section for the participant to sign and date, indicating their agreement to provide informed consent.
09
Ensure the form is reviewed and understood by the participant before signing.
10
Keep a copy of the filled-out form for record-keeping purposes.

Who needs informed consent form adapted?

01
Research organizations conducting scientific studies or clinical trials.
02
Healthcare institutions and hospitals performing medical procedures.
03
Educational institutions conducting experiments or research.
04
Companies and organizations conducting market research or consumer studies.
05
Any situation where it is necessary to obtain informed consent before involving participants in a study or procedure.

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An informed consent form adapted is a document that outlines the process by which participants are informed about the details of a study or procedure, ensuring they understand its risks, benefits, and their rights before agreeing to participate.
Researchers or institutions conducting studies that involve human participants are required to file an informed consent form adapted.
To fill out an informed consent form adapted, one must provide detailed information about the study's purpose, procedures, risks, benefits, confidentiality, and the right to withdraw, then have participants sign the document.
The purpose of the informed consent form adapted is to ensure that participants are fully aware of what their participation involves and to protect their rights and autonomy.
Information that must be reported includes the study's purpose, procedures, potential risks and benefits, confidentiality measures, contact information for questions, and the right to withdraw.
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