New and established companies need to be aware of influential changes that may affect how medical devices, clinical trials or pharmaceutical labeling is delivered.

We aim not to only to be leaders through our products and solutions, but as thought leaders in the market, providing you with all the information and expertise you need to prepare you for today’s labeling challenges as well as for tomorrow’s.

We offer complimentary thought leadership content in the form of webinars, whitepapers and blog posts around the latest regulations in the industry such as EU MDR or FDA UDI. We discuss how to overcome the challenges of being compliant, as well as around topics such as: Local Language Labeling; E-Labeling; Clinical Trials Labeling; Printing Inspection; Controlling Labeling on a Global Scale; IQ, OQ, and PQ; Best Practices in Labeling and more.

EU MDR Best Practices for UDI Data & Product Labeling EU MDR Best Practices for UDI Data & Product Labeling Posted in: Business Analysis, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Project Managers, Supply Chain, Webinar -

Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the best practices for UDI Data & Product Labeling.

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