Can you explain what informed consent means?
Informed consent is the process of obtaining permission from a person before conducting a healthcare intervention or research, ensuring they understand the risks and benefits.
What are the ethical implications of not obtaining informed consent?
Not obtaining informed consent can lead to violations of autonomy, trust, and can result in harm to individuals, both legally and ethically.
How does informed consent apply in medical research?
In medical research, informed consent ensures participants are fully aware of the study's purpose, procedures, risks, and their right to withdraw at any time.
Are there any exceptions to the informed consent requirement?
Yes, exceptions can include emergency situations where obtaining consent is not feasible, or in cases involving certain vulnerable populations.
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