What are the benefits of a GLS and why are MedTech companies considering it now?
PRISYM ID boosts customer service offer with new customer experience team
PRISYM ID joins Siemens Digital Industries Software Solution Partner Program
PRISYM ID, has achieved GS1 certification for the latest version of its PRISYM360 cloud-based labeling solution
FDA 21 CFR Part 11 allows Medical Device and Life Science organizations to use electronic records and signatures in place of paper.
PRISYM ID has implemented a further six new regulated labeling software systems across the medical device and life sciences sectors.
A group of industry experts is set to explore how medical device, clinical trial and pharmaceutical companies can proactively manage labeling risk.
Industry Experts Share Best Practices of Implementing A ‘Validation Ready’ Cloud Based Global Labeling System.
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.
Specialist knowledge, understanding and experience are key to fulfilling the life science and medical device industries’ unique requirements.