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Secondary Use Informed Consent form: Information and template FOR Participants Version Date: February 3, 2020Instructions: The Secondary Use Study Informed Consent Form Template has been designed
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How to fill out wwwwhointtemplates-for-ined-consent-stemplates for ined consent

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How to fill out wwwwhointtemplates-for-informed-consent-formstemplates for informed consent

01
To fill out the WHO templates for informed consent, follow these steps:
02
Download the templates from the www.who.int website.
03
Read the instructions and guidelines provided with the templates.
04
Fill in the details of the research study or medical procedure for which informed consent is required.
05
Include all necessary information such as the purpose of the study, risks and benefits involved, and any alternatives.
06
Make sure to clearly explain the voluntary nature of participation and the right to withdraw consent at any time.
07
Provide space for the participant or their representative to sign and date the consent form.
08
Ensure that the form includes contact information of the researcher or responsible party for any questions or concerns.
09
Review the completed form for any errors or missing information.
10
Obtain appropriate approvals and signatures as required by local regulations.
11
Keep a copy of the consent form for your records and provide a copy to the participant or their representative.

Who needs wwwwhointtemplates-for-informed-consent-formstemplates for informed consent?

01
Anyone involved in conducting research studies or medical procedures that require informed consent can benefit from using the WHO templates. This includes researchers, healthcare professionals, medical institutions, and individuals involved in clinical trials or experimental interventions. The templates help ensure that participants are fully informed about the study or procedure and can make an educated decision regarding their participation.

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wwwwhointtemplates-for-informed-consent-formstemplates refers to standardized templates designed to ensure that individuals provide informed consent for participation in research or medical procedures, outlining the rights and information necessary for making an informed decision.
Researchers, institutions conducting clinical trials, and healthcare providers who involve participants in studies or medical procedures that require informed consent are typically required to file these templates.
To fill out the templates, ensure that all required fields are completed, including participant details, study information, risks and benefits, and any questions regarding the consent process. It's important to review the guidelines provided with the template for specific instructions.
The purpose is to protect participants' rights by ensuring they are fully informed about the study or procedure, thus allowing them to make a voluntary and informed decision regarding their participation.
Information that must be reported includes the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and the participant's right to withdraw without penalty.
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