Where can I apply for medical electrical equipment training?
The European Commission formally adopted the 98/79 / EC Directive (In Vitro Diagnostic Medical Devices Directive, hereinafter referred to as the IVDD Directive) on 27 October 1998 and announced the European Union Bulletin No. L331 of 7 December 1998 on.
hereinafter referred to as IVD) shall comply with this directive to complete the conformity assessment procedures, affixed with the CE mark, to be listed in the EU.
According to the contents of the bulletin, the EU member states must be in June 7, 2000 to complete the implementation of the instructions required by the relevant laws and regulations ordered to amend the order and since December 2003, all members of the EU sales in vitro diagnosis Medical equipment (In Vitro Diagnostic Medical Devices,
