Regulation on Medical Devices Europe (MDR) causes unrest

06 August 2018

Regulation on Medical Devices Europe (MDR) causes unrest	ÄrzteZeitung
A deficit of qualified employees and the reduced number of notified bodies could result in a shortage of new registrations, hindering manufacturers to introduce new products.
This is a post of a scientific or business information. The information given here is checked thoroughly by “Implant-Register”. However we can´t be responsible for the content. Contact the publisher, if you have questions. You may inform us about changes of the information to improve the Register.

Find NEWS and PUBLICATIONS here according to your interests or use the search box.