Experiments that deal with medicines or other materials

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Reference no: EM133793993

Question

Experiments that deal with medicines or other materials used by humans are first tested on laboratory animals, typically rodents. If these tests go well, then the first clinical trials begin using humans, all of whom must provide informed consent to participate in the clinical trial. If a person qualifies for participation in a clinical trial, they will given an "informed consent" document with details about the study, which will include the potential benefits and possible risks, among other details. A clinical trial participant must be very aware of the the details and must participate in the clinical trial voluntarily. Please answer the following questions with brief but thoughtful comments:

1. If you qualified as a possible clinical trial participant, would you consider participating in the clinical trial? Why or Why not.

2. If you decided to participate in the clinical trial what would you expect to learn before signing the informed consent document?

Reference no: EM133793993

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