Join industry experts from PRISYM ID to find out why data level inspection is vital to your labeling process.
Posted in Achieving Regulatory Compliance, Business Analysis, Clinical Trials, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming The Technical Challenges, Pharmaceuticals, Project Managers, Supply Chain, Webinar
A Webinar from the Experts at KPMG & PRISYM ID on Meeting the Updated Timelines for EU MDR.
Join industry experts from PRISYM ID and GS1 to learn about the new GS1 Clinical Trial barcode standards and the benefits of adopting AI (7240).
Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the best practices for UDI Data & Product Labeling.
Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain?
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.
Join PRISYM ID for this free webinar to learn how an effective “touch your label once” strategy for EU MDR labeling can streamline processes and reduce the cost of a global label change.
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.
Watch this 60-minute webinar on how to successfully integrate SAP with your label lifecycle management solution to accelerate your business processes through end-to-end automation.
EU MDR Labeling Compliance: Learn the Lessons from UDI.