The EU’s new MDR that is expected to get live by the mid of 2020, has major consequences for labelling in every single form.
Usually, manufacturers of medical devices get their labelling including Instructions-For-Use (IFU) flyers & content of their website done by separate teams - with the risk of inconsistencies within their content & inadequacies that is often followed by delays in product launch.
However now, with EU’s new MDR, device manufacturers will have a prospect of doing things differently, such as they will be able to make more use of e-labelling & e-IFUs.
Some the key essentials of the new EU MDR affecting enterprise labelling activity are been mentioned below:
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