Shombi Sharp

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  • Shombi Sharp
  • Journal of long-term effects of medical implants
  • 2007
A basic element in the protection of human subjects in clinical trials is the requirement for informed consent. Informed consent, and the particular minimum information that must be provided to subjects, is regulated in the United States by the FDA and by regulatory authorities in other countries. The informed consent document (ICD) provides a basis for(More)
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