Unfortunately this training course is no longer taking place.
Stick or Twist – How do you make the right decision about whether to Transition your products to MDR?
Attend this Medilink Midlands endorsed Professional Development training course on the Medical Device Regulation Transition, delivered by Medilink Midlands member company IMed Consultancy. Taking place on Monday 18th March, so that you can make an informed choice and meet the fast-approaching application deadline of 26th May 2024!
Medical Device and IVD manufacturers are facing a significant deadline on 26 May 2024. After initial publication of the new EU Medical Device Regulations in 2017, the final deadline to decide on whether to transition existing CE Marked Medical Devices to the new is fast approaching.
Manufacturers who have not made a decision to transition their medical devices to meet the requirements of the new European Union regulations and have not taken the relevant steps before the 26 May 2024 deadline, will not be legally able to continue selling their products into the European Union (and potentially other markets including the UK).
This training course will prepare you for understanding whether it may be right for your business to make the decision to (re)certify your medical devices for sale in the EU. The day is focussed on existing manufacturers of medical devices, who currently CE mark their products and will give you practical insights to support your business in making this important decision.
To view the full programme for the day, course overview, target audience, learning outcomes and to view the speakers click here.