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OFFICIAL USE ON Y Doc Name : Informed Consent Form Template Doc Number : 207001 Doc Versions : 1Date : 13 Mar 2018INFORMED CONSENT FORM 1. Study Information Protocol Title: The Impact of Collaborative
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How to fill out informed consent form 1

01
Read the informed consent form thoroughly to understand all the information and details provided.
02
Fill in your personal details such as name, address, contact information, and date of birth.
03
Ensure you fully understand the purpose of the study or activity for which the informed consent form is required.
04
If you have any questions or concerns, seek clarification from the person or organization providing the form.
05
Carefully review any risks or potential benefits associated with participating in the study or activity.
06
In case you are not comfortable with any aspect of the informed consent form, discuss your concerns with the researcher or person in charge before signing it.
07
Sign and date the form to indicate your informed consent to participate in the specified study or activity.

Who needs informed consent form 1?

01
Individuals who are participating in research studies, medical trials, or any other activities that require informed consent from the participants.
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Informed consent form 1 is a document that outlines the risks and benefits of participating in a research study, and is signed by the participant to indicate their understanding and agreement.
Researchers conducting a study involving human subjects are required to file informed consent form 1.
Informed consent form 1 should be filled out by providing clear and concise information about the study, risks, benefits, and potential outcomes, and ensuring that the participant understands and agrees to the terms.
The purpose of informed consent form 1 is to ensure that participants are fully informed about the study, including its risks and benefits, before agreeing to participate.
Information such as study objectives, procedures, risks, benefits, confidentiality, and contact information for questions must be reported on informed consent form 1.
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