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------- Research Ethics Review Committee (WHO ERC) 20, AVENUE APIA CH-1211 GENEVA 27 SWITZERLAND HTTP://INTRANET.WHO.INT/HOMES/RPC/ERC HTTP://WWW.WHO.INT/RPC/RESEARCH ETHICS Informed Consent Form

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What is informed consent form template?

An informed consent form template is a standardized document that outlines the necessary information provided to individuals before they participate in a research study or medical procedure. It ensures that participants understand the risks, benefits, and procedures involved and gives them the opportunity to make an informed decision about their participation.

Who is required to file informed consent form template?

Researchers, healthcare providers, and institutions conducting research or medical procedures that involve human subjects are required to file an informed consent form template. This ensures that participants are fully informed and have given their voluntary consent to participate in the study or procedure.

How to fill out informed consent form template?

Filling out an informed consent form template involves providing the necessary information about the study or procedure, including its purpose, potential risks and benefits, procedures involved, confidentiality measures, and contact information for any inquiries. Additionally, participants must provide their signature to indicate their voluntary consent to participate.

What is the purpose of informed consent form template?

The purpose of an informed consent form template is to protect the rights and well-being of individuals participating in research studies or medical procedures. It ensures that participants are fully informed about what they are consenting to, including any potential risks and benefits. It also allows them to ask questions, seek clarification, and make an informed decision before participating.

What information must be reported on informed consent form template?

An informed consent form template must include information about the study or procedure, its purpose, potential risks and benefits, procedures involved, confidentiality measures, contact information for any inquiries, and any compensation or incentives offered to participants. It should also inform participants of their rights, including the ability to withdraw from the study at any time without penalty.

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