How are medical devices regulated in the European Union?

J R Soc Med. 2012 Apr;105 Suppl 1(Suppl 1):S22-8. doi: 10.1258/jrsm.2012.120036.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Credentialing* / legislation & jurisprudence
  • Credentialing* / standards
  • Device Approval* / legislation & jurisprudence
  • Device Approval* / standards
  • Equipment Safety* / classification
  • Equipment Safety* / standards
  • Equipment and Supplies / classification
  • Equipment and Supplies / standards
  • European Union
  • Government Regulation
  • Humans
  • Industry / legislation & jurisprudence*
  • Industry / standards*
  • International Cooperation / legislation & jurisprudence*
  • Legislation, Medical / organization & administration
  • Product Surveillance, Postmarketing / standards
  • Reference Standards