European Authorized RepresentativeandConsulting services
for manufacturers of Medical Devices
CEpartner4U offers independent and confidential services for the CE-marking under EU Medical Device Directives.
New MEDDEV document concerning classification of medical devices
EU-wide databank (EUDAMED) for medical devices to boost market surveillance
Issuance of Guidance on NB's Tasks of Technical documentation Assessment
New MEDDEV document concerning borderline products (drug delivery / medical devices)
Issuance of interpretative document of 2007/47/EC which amends the Medical Device Directive
