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
PRISYM ID BOOSTS CUSTOMER SERVICE OFFER WITH NEW CUSTOMER EXPERIENCE TEAM PRISYM ID boosts customer service offer with new customer experience team Read More
PRISYM ID joins Siemens Digital Industries Software Solution Partner Program as a Software and Technology Partner PRISYM ID joins Siemens Digital Industries Software Solution Partner Program Read More
PRISYM ID underlines its commitment to patient safety with updated GS1 certification PRISYM ID, has achieved GS1 certification for the latest version of its PRISYM360 cloud-based labeling solution Read More
What is FDA 21 CFR PART 11 Posted on 5th June 2021 by Jack Cowmeadow FDA 21 CFR Part 11 allows Medical Device and Life Science organizations to use electronic records and signatures in place of paper. Read More
PRISYM ID announces six further projects go live as medical device and life science organizations prepare for the future PRISYM ID has implemented a further six new regulated labeling software systems across the medical device and life sciences sectors. Read More
Experts to come together for compliance event exploring ‘validation ready’ global labeling systems A group of industry experts is set to explore how medical device, clinical trial and pharmaceutical companies can proactively manage labeling risk. 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
EU MDR Checklist Ahead of its introduction on 26 May 2021, here is a practical checklist outlining some of the key elements you should consider to ensure your business operation is fully compliant with EU MDR. Read More