Service
CE marking for Medical Devices and In Vitro Diagnostic Medical Devices
Establishment of QMS according to ISO13485 Preparation of technical documentation
Sr. Project Manager Medical Devices
Holland Innovative
Eindhoven, Netherlands
Service
CE marking for Medical Devices and In Vitro Diagnostic Medical Devices
Establishment of QMS according to ISO13485 Preparation of technical documentation
Expertise
(In vitro diagnostic) medical devices: regulatory expertise
Regulatory advice for manufacturers of (in vitro diagnostic) medical devices; from D&D through verification/validation to the market
Expertise
Establishment and implementation quality management system compliant with ISO13485