How to Successfully Manage Compliance for EU MDR
European Union's Medical Device Regulation (EU MDR) is clearly a priority for everyone in the medical device industry. As many of you know, the enforcement of the first milestone takes effect in May of 2020. As the deadline approaches, manufacturers and suppliers are forced to comply with pending changes quickly or be faced with major implications of their business.The following report outlines a path to compliance and how to:
- Identify if your company is on course for compliance
- Overcome the 11 new label elements on a global scale
- Manage the impact of import and export on labeling
- Avoid recalls and non-compliance
- Futureproof your labeling and packaging artwork
Learn how companies are embracing more advanced, automated labeling and artwork management solutions in order to achieve EU MDR compliance.
About Loftware
Loftware is the global leader in Enterprise Labeling and Artwork Management solutions offering the industry’s most comprehensive digital platform to create, manage and print complex labeling and packaging artwork and scale across global operations.
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