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Origen Biomedical PRISYM ID helps OriGen Biomedical to Automate their Processes and Achieve Regulatory Compliance Posted in: Achieving Regulatory Compliance, Business Analysis, Coverage, Medical Device, Operations & Labeling, PRISYM SaaS - Medical device manufacturer, OriGen Biomedical, has selected PRISYM ID’s label management solution to put data at the heart of its…
Single-Touch Labeling Single-Touch Labeling: the Answer to EU MDR? Posted in: Achieving Regulatory Compliance, Business Analysis, Coverage, Medical Device - Warren Ward-Stacey, PRISYM ID , examines a single-source approach that could eradicate data duplication, inconsistencies, and costly human error
Christmas 300x197 - Happy Holidays! Happy Holidays! Posted in: Coverage - We would like to wish all of our customers, partners and suppliers a very Merry Christmas and a Happy and…
PRISYM 360 Brochure PRISYM ID announces 1.8 Release for its Life Science Dedicated Labeling Solution, PRISYM 360 Posted in: Clinical Trials, Coverage, Medical Device, PRISYM 360 - Release 1.8 of PRISYM 360 introduces new features to help medical device and clinical trials organizations to achieve complete label…
EU MDR A Sticky Situation: Will your Labels Comply with EU MDR? Posted in: Achieving Regulatory Compliance, Business Analysis, Coverage, Medical Device - Mark Cusworth, PRISYM ID, examines EU Medical Device Regulation and its implications on labeling highlighting the requirements for the new…
LPP PRISYM ID Launches New Partnership Program Posted in: Clinical Trials, Medical Device, Pharmaceuticals, Press Releases, PRISYM 360 - We are delighted to announce the launch of our exciting Lifetime Partnership Program (LPP), which aims to achieve the successful…
Medical Device EU MDR: The nightmare before Christmas? – MedTech Innovation Posted in: Achieving Regulatory Compliance, Business Analysis, Coverage, Medical Device - Mark Cusworth, PRISYM ID, examines EU Medical Device Regulation and its implications on labeling – and looks ahead to a…
New website 300x195 - PRISYM ID Launches New Website! PRISYM ID Launches New Website! Posted in: Press Releases - We are delighted to announce that we have launched our new website, which can still be found at www.prisymid.com.
Best Practice 2 300x225 - Best Practice Guidance for UDI Compliance – published in Med-Tech Innovation Best Practice Guidance for UDI Compliance – published in Med-Tech Innovation Posted in: Coverage - The system means that by 2020 most medical devices will need to include a Unique Device Identifier (UDI) in human…
Zebra 300x225 - PRISYM ID Achieves Zebra Technologies Validation PRISYM ID Achieves Zebra Technologies Validation Posted in: Clinical Trials, Medical Device, Pharmaceuticals, Press Releases, PRISYM 360 - PRISYM 360 validated at Zebra’s Solutions Center to revolutionize label lifecycle management
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