- This course has passed.
Medical Device Regulations (MDR)
Introduction to the MDR one day training
The legislation outlining the requirements for medical device manufacturers prior to placing them on the market in the European Union is changing. The old Medical Devices Regulation (EU 2017/745) is to be replaced by the Medical Devices Directive (93/42/EEC). The new regulations place greater emphasis on accountability for all players and with greater scrutiny of both clinical evaluation and post-market clinical evaluations and improved traceability of devices for the full life cycle.
Who should attend this training:
Those with a working knowledge QMS from all levels within the organisation including (but not limited to):
• Authorised Representatives
• Manufacturing personnel
• Regulatory Affairs
• Design and Development
• Economic Operators for example importers and distributors
Need a quote for in-house training email firstname.lastname@example.org
phone +353 (0) 1-2040646
Tickets are not available as this course has passed.