Medical Devices Regulatory (MDR) Talk
How ready are you for the Medical Devices Regulation?
The Medical Devices Regulation (MDR) (EU 2017/745) has replaced the Medical Devices Directive (MDD) (93/42/EEC) as the legislation detailing the requirements that medical device manufacturers have to meet to place medical devices in the EU market. The first part of the talk will share on the changes in MDR compared to MDD and how would these changes affect the medical device manufacturers placing their products in Europe. This session will also cover the introduction of Unique Device Identification (UDI).
The second half of the talk will focus on compliance timeline. Getting ready to go through conformity assessment and to successfully transit from MDD compliance to MDR, including some common examples for the transition.
Join us on Friday, 19 July at 9:30am for the talk and learn more about the changes, compliance timeline and conformity assessment by BSI expert, Mr. Francesco Laterza all the way from Italy.