Why you should take advantage of the AI (7240) and adopt the new GS1 Clinical Trial barcode standards Posted in: Achieving Regulatory Compliance, Business Analysis, Clinical Trials, Increasing The Operational Efficiency, Information Technology, Operations & Labeling, Overcoming The Technical Challenges, Project Managers, Supply Chain, Webinar - Join industry experts from PRISYM ID and GS1 to learn about the new GS1 Clinical Trial barcode standards and the… 
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… 
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 - Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain? 
Medical Device: How to Identify, Address and Remove the Risks of Labeling Product Recalls Posted in: Achieving Regulatory Compliance, Business Analysis, Medical Device, Regulatory & Compliance, Webinar - Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the latest recalls trends… 
PRISYM SaaS Demo: Validated Labeling for Small-to-Medium Medical Device Manufacturers Posted in: Medical Device, Webinar - Join us for our demo to see how our validated labeling solutions have been helping organizations to achieve regulatory compliance,… 
EU MDR Labeling – ‘Touch Your Label Once’ Strategy Posted in: Achieving Regulatory Compliance, Medical Device, Regulatory & Compliance, Webinar - Join PRISYM ID for this free webinar to learn how an effective “touch your label once” strategy for EU MDR… 
EU MDR’s Impact on Labeling: UDI in Europe and Other Changes Posted in: Achieving Regulatory Compliance, Medical Device, Regulatory & Compliance, Webinar - Join medical device labeling and data experts from PRISYM ID and Reed Tech to learn about what the EU Medical… 
Integrating Labeling with SAP for Label Content Integrity and Control Posted in: Webinar, Increasing The Operational Efficiency, Information Technology, Operations & Labeling, Overcoming The Technical Challenges - Watch this 60-minute webinar on how to successfully integrate SAP with your label lifecycle management solution to accelerate your business… 
EU MDR Labeling Compliance: Learn the Lessons from UDI Posted in: Achieving Regulatory Compliance, Business Analysis, Increasing The Operational Efficiency, Information Technology, Medical Device, Operations & Labeling, Overcoming The Technical Challenges, Project Managers, Regulatory & Compliance, Webinar - EU MDR Labeling Compliance: Learn the Lessons from UDI. 
UDI and the EU MDR: What you Need to Know to Comply Posted in: Webinar, Achieving Regulatory Compliance, Medical Device, Regulatory & Compliance - Labeling Webinar Series - A Date with the Experts on Global Labeling Systems. 
