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PW ANI UNIVERSITY ETHICS REVIEW COMMITTEE TEMPLATE OF INFORMED CONSENT FORM Title of Project: Insert Title Name of Researcher: Insert Name Please initial box I confirm that I have read and understood
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To fill out the template of informed consent, follow these steps:

01
Begin by including the relevant information of the individual providing the consent, such as their name, address, and contact details.
02
Clearly state the purpose of the informed consent, outlining the nature of the activity or procedure for which consent is being obtained.
03
Specify any potential risks or benefits associated with the activity or procedure, ensuring that they are explained in a clear and understandable manner.
04
Include a section for the individual to indicate their understanding of the information provided, ensuring that they have had the opportunity to ask any necessary questions.
05
If necessary, provide space for the individual to indicate any special considerations or conditions that should be taken into account during the activity or procedure.
06
Clearly state whether the individual has the right to withdraw their consent at any time, and provide instructions on how to do so.
07
Include a signature line for the individual, as well as a date field to indicate when the consent was provided.
The template of informed consent is typically needed by individuals or organizations conducting activities or procedures that require explicit permission from participants or patients. This may include medical professionals obtaining consent for a specific treatment, researchers requiring consent for participation in a study, or organizations obtaining consent for the use of an individual's personal information.
By utilizing the template, all relevant information can be documented and easily understood, ensuring that informed consent is obtained in a clear and standardized manner.
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The template of informed consent is a standardized form that outlines the information provided to individuals before they decide to participate in a research study or medical treatment.
Researchers, healthcare providers, and institutions conducting studies or providing treatments that involve human subjects are required to file a template of informed consent.
The template of informed consent should be filled out by including all relevant information about the study or treatment, potential risks and benefits, confidentiality measures, and participant rights.
The purpose of the template of informed consent is to ensure that individuals have all necessary information to make an informed decision about participating in a study or treatment.
The template of informed consent must include details about the study or treatment, risks and benefits, confidentiality measures, participant rights, and contact information for questions or concerns.
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