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On March 21, 2018, the U.S. House of Representatives passed a bill allowing patients the right to try experimental drugs prior to FDA approval. Discuss the ethical principles of beneficence (doing good) and of non-maleficence (avoiding causing harm) and issues of the morality of a legal system that delays research because of the legal rights of patent holders. In replies to peers, describe how you would handle this ethical issue with your patients.
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