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The principle that participants in research must be fully aware of the nature, risks, and benefits of the study and provide their consent before participating.
The duty to promote the well-being and benefit of research participants, ensuring that the research does not harm them and that it contributes to the greater good.
The principle of doing no harm, ensuring that research does not cause physical or psychological harm to participants.
The respect for participants’ right to make decisions about their own bodies and lives, including the right to refuse participation or withdraw from a study.