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 complementary thought leadership content in the form of webinars, whitepapers and blog posts around the latest regulations in the industry such as MDR or 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 EU MDR’s Impact on Labeling: UDI in Europe and Other Changes Posted in: Achieving Regulatory Compliance, Business Analysis, Medical Device, Operations & Labeling, Project Managers, Reducing Risks, Regulatory & Compliance, Supply Chain, Webinar -

Join medical device labeling and data experts from PRISYM ID and Reed Tech to learn about what the EU Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR) mean for labels in this free webinar.

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