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Consent Policy Introduction The purpose of this policy is to set out the Practices approach to consent and the way in which the principles of consent will be put into practice. Where possible, a clinician
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01
Explain the research study thoroughly to the participant, making sure they understand the purpose and procedures involved.
02
Clearly outline the potential risks and benefits of participating in the study.
03
Ensure the participant has ample time to ask questions and fully comprehend the information provided.
04
Obtain the participant's voluntary agreement to participate in the study by having them sign the informed consent form.
05
Provide a copy of the signed informed consent form to the participant for their records.

Who needs informed consent an ethical?

01
Informed consent is ethically required for any individual participating in a research study or clinical trial.
02
It ensures that participants are fully informed about the study and voluntarily agree to take part in it.
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Informed consent is ethical because it ensures that individuals are fully informed about the risks and benefits of participating in a research study or medical procedure, allowing them to make a voluntary and educated decision.
Researchers, healthcare providers, and other professionals who are conducting studies or procedures that involve human subjects are required to obtain and file informed consent.
To fill out informed consent, you must provide information about the study or procedure, including its purpose, potential risks and benefits, alternative options, confidentiality, and the participant's rights. The participant must then sign the form to indicate their understanding and willingness to participate.
The purpose of informed consent is to protect the rights and well-being of individuals participating in research studies or medical procedures. It also ensures transparency and trust between researchers/healthcare providers and participants.
Informed consent forms typically include information about the study or procedure, its purpose, potential risks and benefits, alternative options, confidentiality, the participant's rights, and contact information for questions or concerns.
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