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the goal today will be to better understand informed consent in medicine and theres two contexts in particular that were going to be looking at were going to be looking at what does it mean to secure informed consent in a clinical setting where a physician is treating a patient and what does it mean to secure informed consent in an experimental setting where researchers are conducting tests on test subjects now theres going to be a lot of overlap in terms of what informed consent means in each of these contexts but in the clinical setting you might say that the primary goal is to treat the patient to help the patient get better to improve their health whereas in the experimental setting the primary goal is going to be directed more towards gaining knowledge gaining an understanding of what sorts of treatments work and which sorts of treatments dont work so because the goals are going to be a little bit different again the clinical setting is about healing and treatment and the exp
