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How Are Medical Device Companies Addressing EU MDR?
Label and packaging artwork processes play an important role in meeting compliance for EU MDR.
With the next major milestone for EU MDR fast approaching, many medical device companies are finding they need to make some quick decisions to address the range of issues presented by this looming deadline.
Part of the challenge involves reassessing their label and packaging artwork processes to ensure compliance. And, EU MDR doesn’t discriminate: Whether you’re a large global manufacturer or a small player in the medical device space, these pending changes will impact any business residing in or selling into the European market, so it will have major implications for businesses of all sizes.
MedTech Intelligence recently posed some questions around EU MDR preparedness to a few of Loftware’s medical device experts. Loftware’s Laura Johnson explains the important role that label and packaging artwork processes play in meeting compliance for EU MDR.
- Regulatory
- UDI
- Supply Chain
- Artwork Management
- Labeling
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