How to Successfully Manage Compliance for EU MDR
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.
Medical device companies first need to understand the requirements for successful compliance. The new rules mandate a complete redesign of all labels for medical devices targeting the European market. To accomplish this, it would be impractical for companies to rely on age-old legacy labeling processes and systems.
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.
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