Answer:
Informed consent.
Explanation:
Informed consent simply means a decision taken by or for an individual after being informed about the proposed research or procedures, risks, benefits, and details about a research or procedures.
There need to be or have a legal informed consent if you have described to your patient or participants the research or procedure you are going to do in detail.
The features of the informed consent process.
1. The act of learning the key informations about a clinical trial before deciding whether or not to participate.
2. It helps individuals to agree or disagree in participating, health care providers involved in the trial explain the details of the study and others.
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