Pharmaceuticals and Medical Devices: FDA Oversight

Issue Brief Health Policy Track Serv. 2016 Dec 27:2016:1-59.
No abstract available

MeSH terms

  • Centers for Medicare and Medicaid Services, U.S.
  • Commerce
  • Computer Security
  • Device Approval / legislation & jurisprudence*
  • Electrical Equipment and Supplies
  • Equipment Failure
  • Equipment Safety
  • Equipment and Supplies / adverse effects*
  • Europe
  • Fees and Charges / legislation & jurisprudence
  • Fraud / legislation & jurisprudence
  • Genetic Markers
  • Genetic Testing / instrumentation
  • Genomics / instrumentation
  • Government Regulation*
  • Health Services Accessibility
  • Humans
  • Mandatory Reporting
  • Medicare / economics
  • Medicare / legislation & jurisprudence
  • Monitoring, Ambulatory / instrumentation
  • Patents as Topic / legislation & jurisprudence
  • Privacy / legislation & jurisprudence
  • Product Recalls and Withdrawals / legislation & jurisprudence
  • Professional Misconduct
  • Surgical Mesh / adverse effects
  • Transplants
  • United States
  • United States Food and Drug Administration / legislation & jurisprudence
  • Zika Virus Infection / diagnosis

Substances

  • Genetic Markers