Medical Devices CE Marking
Our “Medical Devices CE Marking” three-day training course is designed to provide participants with the knowledge to assist their companies in getting products to market more quickly.
Management personnel responsible for all aspects of CE marking medical devices as well as internal and external auditors will benefit from this course.
Participants will gain knowledge of the requirements of the Medical Device Directive and the CE Marking approach. Participants will be able to provide leadership for their organizations when placing medical devices on the market in the European Union.