Do you manufacture class III medical devices?
If yes, are you ready for the 24 September deadline? Watch our recent webinar with Jay Crowley for a step by step guide to FDA UDI compliance.
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Our validatable solutions offer Life Sciences Organisations' complete label integrity to support with compliance requirements such as US FDA & EU regulations.
Gain a 360 Degree View of Your Label Lifecycle Management
Our expert team regularly host complimentary webinars that share best practice labeling tips for the highly regulated Life Sciences Industry
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67% of labeling defects occur during the print process due to human error. Discover how this can be avoided through implementing an automated label inspection system.
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