Assignment:
Write an explanation of how informed consent for medical research (clinical trials) differs from the patient's consent to treat used in health care practice (e.g., medical treatment or surgery). Explain why you think this difference exists? Provide at least one clear example of how informed consent could be used in medical research and one example of how it is used in health care practice. Then provide an example of each of the four ethical principals in action in research. Use credible resources to support your answer.
Your answer must be in 350 to 400 words, typed, double-spaced, Times New Roman font (size 12), one-inch margins on all sides, APA format.