Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain?
Are you struggling to implement an on-demand packaging model…
Mark Cusworth, VP of Research and Development at PRISYM ID examines the EU Medical Device Regulation and its implications on labelling
Craig Jones, VP enterprise sales engineering, PRISYM ID, shares how to avoid costly and inefficient labeling recalls
Mark Cusworth, PRISYM ID, examines The ten steps to labeling implementation for both SMEs and large enterprises – article published in Manufacturing Chemist
Steve Ellison, PRISYM ID, examines The Battle Against Counterfeit Medical Devices – article published in MedTech Intelligence
Medical device manufacturer, OriGen Biomedical, has selected PRISYM ID’s label management solution to put data at the heart of its medical device labeling processes.
Discover how PRISYM ID helped Origen Biomedical, a growing medical device manufacturer, who was looking for a cost effective and easy to use label printing process.
Posted in Achieving Regulatory Compliance, Assisting With The Consolidation, Business Analysis, Case Study, Enabling the Expansion, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming The Technical Challenges, Project Managers, Reducing Risks, Regulatory & Compliance
Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the latest recalls trends from the industry, to see how the right software platforms can minimize the risks of labeling recalls.
Warren Ward-Stacey, PRISYM ID , examines a single-source approach that could eradicate data duplication, inconsistencies, and costly human error
We like to make our webinars interactive and after our recent webinar on ‘EU MDR’s Impact on Labeling: UDI in Europe and Other Changes’, I thought it would be great to highlight the top five challenges and questions we saw strong responses to