Federal Policies and the Medical Devices Industry
Health Program (J. E. Sisk)
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Guidance for Industry: Good Reprint Practices for the Distribution of Medical Journal Articles and Medical or Scientific Reference Publications on Unapproved New Uses of Approved Drugs and Approved or Cleared Medical Devices Unknown author (United States. Department of Health and Human Services. Food and Drug Administration [FDA]. Office of the Commissioner, Office of Policy, 2009-01)