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Joint Research Compliance Office This is a controlled document. The master document is posted on the JRC website and any print off of this document will be classed as uncontrolled. Researchers and
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How to fill out informed consent for research

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Step 1: Read the informed consent form thoroughly to understand the purpose, risks, benefits, and procedures involved in the research.
02
Step 2: Ask any questions or seek clarification from the researchers before proceeding.
03
Step 3: Evaluate the information provided and ensure you have a clear understanding of what is being asked and expected from you as a participant.
04
Step 4: Discuss the research and its potential impact with family members or trusted individuals to make an informed decision.
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Step 5: If you decide to participate, sign and date the informed consent form.
06
Step 6: Retain a copy of the signed consent form for your personal records.
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Step 7: Follow any additional instructions provided by the researchers for participating in the research.

Who needs informed consent for research?

01
Anyone who is being asked to participate in a research study needs informed consent. This includes potential participants who are adults, minors, or individuals with cognitive impairments. Informed consent ensures that individuals have the necessary information to make an autonomous decision regarding their participation in the research.
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Informed consent for research is a process in which individuals voluntarily agree to participate in a study after being provided with relevant information about the research, including potential risks and benefits.
Researchers are required to obtain and file informed consent from participants before conducting any research.
Informed consent forms must be filled out by providing participants with all necessary information about the research study and obtaining their voluntary agreement to participate.
The purpose of informed consent for research is to protect the rights and welfare of research participants by ensuring they have the necessary information to make an informed decision about whether or not to participate.
Informed consent forms must include details about the study's objectives, procedures, risks, benefits, confidentiality, and the participant's right to withdraw from the study at any time.
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