What makes consent voluntary in context of clinical trials

Reference no: EM133617398

Question

If Stephanie's parents object to her inclusion in the Stage III trial, even if it might in the end benefit Stephanie, is there any way that Stephanie can still be enrolled in the research? Why or why not? If necessary parties all agree that Stephanie's participation might be a good medical option, are there any concerns with the "voluntariness" of this decision? If so, what are they and how might the concerns be minimized/mitigated/addressed? If not, explain what makes consent voluntary in the context of clinical trials for pharmaceuticals.

Reference no: EM133617398

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