Live: One Dial-in One Attendee
Corporate Live: Any number of participants
Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
The EU Medical Device Regulation (MDR 745/2017) represents a considerable change from the directives it is replacing.
Device manufacturers who conduct business in the EU must start their transition now in order to meet the deadline.
This training is the first peek into this uncharted realm. During this class participants will be introduced to the new requirements in the Medical Device Regulation (MDR), including those related to quality systems, product classification rules, technical documentation, clinical evaluations, Unique Device Identification (UDI), and postmarket surveillance. Also, learn how to plan an efficient transition.
In May 2017 the European Union has released its new regulation concerning Medical Devices. This regulation introduces many challenges to the Medical Devices industry.
Why you should Attend: One should attend, in order to start understanding what the new challenge and ways are to handle it. How to establish the correct strategy? What is newly adopted as a requirement, and what?
Areas Covered in the Session: