After the Holocaust, a set of Laws was set as the standard for medical and research ethics, thus the Nuremberg Code. In a 1953 Document, the Nuremberg Code is presented, followed by this statement, “Much the same rules in regard to medical experiments on human beings have been delineated by the American Medical Association” (Shimkin 401-403). The Nuremberg Code was a response to the atrocities that occurred in Europe during the Holocaust, and the main function of the Code was to clearly state what was legal and illegal in the field of medicine with humans as subjects, because “Research on human beings, of course, involves unique hazards, precautions, and responsibilities…ethical, religious, and legal considerations, cannot and must not be ignored or minimized” (Shimkin 401). Other regulatory groups and systems have been put into play in order to make sure these considerations are not ignored; these include the FDA and the U.S. Department of Health and Human Services among many others. These governmentally funded groups as well as others have been the reason for protections and standards of care that must be met when it comes to human experimentation, medical testing, and the healthcare…
