PRISYM ID want to let you know how we are responding to the challenge thrown down by Covid-19 and how we can best help your organisation.
With just a few months to go before EU MDR officially becomes law, the medical device industry’s collective preparedness for it remains surprisingly patchy.
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.
PRISYM ID introduces an InDesign Plugin to its life science dedicated label and artwork management platform, PRISYM 360.
PRISYM ID’s compliant labelling solution, PRISYM 360, has been selected by CME Ltd to ensure delivery of just in time clinical trials for the Medicines Manufacturing Innovation Centre project.
PRISYM ID will be exhibiting and hosting a workshop at this year’s American Medical Device Summit on October 28-29, 2019.
PRISYM ID will be exhibiting at the Clinical Trial Supply East Coast 2019 on the 16th and 17th of October, in King of Prussia, booth 16.
PRISYM ID will be attending this years RAPS Regulatory Convergence on September, 22-24 2019 in Philadelphia.
PRISYM ID will proudly be exhibiting at this year’s Pharma and Device Packaging and Labelling Europe event on 10th and 11th September 2019.