If a patient expresses interest in the study; therefore, it is the contractual obligation of the medical or research colleague to go over the informed consent involving potential risks, benefits, and requirements of participation. The key point are clinical trial sites, summarize the elements of an informed consent practice, and offers helpful instruction on conducting the informed consent procedure. The strong point of this article is that the authors have excellent information on understanding the uncertainty about their results and the drawbacks of body awareness. A professional can aid clients in getting actively engaged and involved in their own concern. The strong point of this article is the authors show an example of a basic informed consent form. I believe the weaknesses of this article is the authors should have received feedback from patients who understood informed consent or …show more content…
The key points are, people can give informed consent only if they are competent to act thus. An informed consent procedure in medicine is that they are useless for selecting public health. Informed consent is that medical treatment of the individual’s user’s personal data, about third parties that is divulged without consent. Informed consent emerges when people with adequate competence to consent, or under duress or constraint, so less able refuse others demands. The strong point of this article is the author’s discussions many limitations of using informed consent. I wish that author compare everyday transactions to informed consent. The failings of this article or maybe the writer could have given more examples of what was not acceptable. I remembered the article was real interesting because people truly do not know the limitation of informed consent. The article is significant because it presents many details on informed consent and respecting patient autonomy. Overall, I will be more conscious for patient and myself on informed consent procedures, which protects our