Reporting standards for adverse events after medical device use in the peripheral vascular system

J Vasc Surg. 2013 Sep;58(3):776-86. doi: 10.1016/j.jvs.2013.06.059.
No abstract available

Publication types

  • Practice Guideline
  • Review

MeSH terms

  • Clinical Trials Data Monitoring Committees / standards
  • Clinical Trials as Topic / legislation & jurisprudence
  • Clinical Trials as Topic / standards*
  • Clinical Trials as Topic / statistics & numerical data
  • Data Interpretation, Statistical
  • Endovascular Procedures / adverse effects
  • Endovascular Procedures / instrumentation*
  • Equipment Design
  • Ethics Committees / standards
  • Ethics Committees, Research / standards
  • Government Regulation
  • Humans
  • Peripheral Vascular Diseases / surgery
  • Peripheral Vascular Diseases / therapy*
  • Product Surveillance, Postmarketing / standards*
  • Product Surveillance, Postmarketing / statistics & numerical data
  • Research Design / legislation & jurisprudence
  • Research Design / standards*
  • Research Design / statistics & numerical data
  • Terminology as Topic