European Authorized RepresentativeandConsulting services
for manufacturers of Medical Devices
CEpartner4U offers independent and confidential services for the CE-marking under EU Medical Device Directives.
More information soon!
Online survey to determine the need for modification or updating of ISO 13485:2003 requirements standard and ISO/TR 14969:2004 guidance document
Restriction of Hazardous Substances (RoHS) Recast Update
New MEDDEV document concerning classification of medical devices
