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.
Are you Ready for the Annex VI EU No 536/2014 Labeling Changes? Posted in: Business Analysis, Clinical Trials, Increasing The Operational Efficiency, Information Technology, Operations & Labeling, Overcoming The Technical Challenges, Project Managers, Supply Chain, Webinar - 
