EU Commission to give more time for MDR transition
A proposal meant to mitigate potential medical device shortages under the Medical Device Regulation is now headed to the European Parliament and Council under an accelerated procedure.
by ulrich quistgaard, translated by daniel pedersen
The EU Commission has adopted a proposal for staggered deadlines in the implementation of the Medical Device Regulation, MDR, meaning that devices, depending on their risk classifications, will have more time before new certification is required.
Already a subscriber?Log in here
Read the whole article
Get access for 14 days for free. No credit card is needed, and you will not be automatically signed up for a paid subscription after the free trial.
With your free trial you get:
- Access all locked articles
- Receive our daily newsletters
- Access our app
Get full access for you and your coworkers
Start a free company trial todayRelated articles:
Ambu credits MDR milestone to fastidiousness
For subscribers
