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INFORMED CONSENT DECLARATION FORM NB Patient/Client/Carer/Colleague/Staff column should be completed by using a Code e.g. Client A/Patient A. Client B etc in order to preserve anonymity and confidentiality.
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Step 1: Begin by reading the informed consent declaration form thoroughly to understand its contents and purpose.
02
Step 2: Write your name and contact information in the designated fields provided on the form.
03
Step 3: Carefully review the information about the research study or medical procedure for which you are providing consent.
04
Step 4: Seek clarification from the researcher or healthcare professional regarding any questions or concerns you may have about the study or procedure.
05
Step 5: Sign and date the form to indicate your informed consent. Ensure that you have understood the information and voluntarily agreed to participate or undergo the medical procedure.
06
Step 6: Keep a copy of the fully completed informed consent declaration form for your records.

Who needs informed consent declaration form?

01
The informed consent declaration form is needed by individuals who are participating in a research study or undergoing a medical procedure. It is a legal document that ensures individuals fully understand the risks, benefits, and purpose of the study or procedure and willingly provide their consent to participate or undergo the procedure.
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The informed consent declaration form is a document that outlines the details and implications of a research study that participants must read and sign before participating.
Researchers and study personnel conducting a research study are required to have participants sign the informed consent declaration form.
The informed consent declaration form must be filled out by providing accurate information about the research study, potential risks and benefits, and participant rights.
The purpose of the informed consent declaration form is to ensure that participants are fully informed about the research study, its implications, and their rights before deciding to participate.
The informed consent declaration form must include details about the research study, potential risks and benefits, participant rights, and contact information for questions or concerns.
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