The deadline to the EU Medical Device Regulation directive is approaching. The EU MDR will replace the current AIMDD and MDD and by May 26, 2020 all medical device manufacturers will need to be compliant. (On April 3, 2020, the European Commission decided to postpone the MDR Deadline for one year to give medical device companies a chance to focus on the current COVID-19 pandemic)
The new regulation will affect all aspects of the supply chain, including the need to translate content into languages accepted by the different European Union states.
Prepare yourself now for the new MDR with our FREE Whitepaper!
Download our whitepaper to find the answers to frequently asked questions, including:
- How do the regulations differ for devices that are intended for use by patients vs medical professionals?
- What additional content must be translated as a result of the MDR changes?
- Are there any restrictions to what type of symbols we can use?