• Identify relevant ethical theories and moral principles.
  • Explain how the principle of informed consent is relevant to the issue.
  • Explain the costs and benefits of making unproven, unapproved experimental drugs widely available to patients. Consider the costs and benefits not only to the individual patients who take these drugs but also potential costs and benefits to other patients.
  • Explain arguments using examples for and against offering pre-approved drugs to wider pools of patients.
  • Support your view using ethical theories or moral principles (or both) that you find most relevant to the issue.