Why Medical Device Manufacturers Must Look at the Bigger Picture When Implementing a GLS What are the benefits of a GLS and why are MedTech companies considering it now? Read More
Why a Global Labeling System is becoming critical for Medical Device Manufacturers What are the benefits of a GLS and why are MedTech companies considering it now? Read More
True Validation ‘Ready’ Labeling – What It Really Means Industry Experts Share Best Practices of Implementing A ‘Validation Ready’ Cloud Based Global Labeling System. Read More
RxSource Shares Advice on Optimizing Labelling Processes Join industry experts from PRISYM ID and RxSource to explore the key areas to optimizing your labelling and packaging processes. Read More
Push the Button on Content ‘Mass Change’ Events & Labeling Simplify and Standardize your Approach to Managing Content Changes to Regulated Labels, Multi-page Documents and IFUs. Read More
Labeling Scrutinized – The Importance of Inspection Join industry experts from PRISYM ID to find out why data level inspection is vital to your labeling process. Read More
The Clock is Reset…Opportunity for your Organization to Re-Evaluate compliance to EU MDR Labeling A Webinar from the Experts at KPMG & PRISYM ID on Meeting the Updated Timelines for EU MDR. Read More
Why you should take advantage of the AI (7240) and adopt the new GS1 Clinical Trial barcode standards 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). Read More
EU MDR Best Practices for UDI Data & Product Labeling Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the best practices for UDI Data & Product Labeling. Read More
Are you Ready for the Annex VI EU No 536/2014 Labeling Changes? Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain? Read More
