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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
Labelling Matters 300x225 - Labeling Matters Labeling Matters Posted in: Coverage - While not front of mind in drug development, the packaging and, in particular, labelling of medicines are the final pieces…
PRISYM ID joins 300x225 - PRISYM ID joins SAP® PartnerEdge® Program “Build” Model PRISYM ID joins SAP® PartnerEdge® Program “Build” Model Posted in: Press Releases - PRISYM ID also announces Integration of its PRISYM 360 Label Lifecycle Management Platform with SAP NetWeaver® PRISYM ID today announces…
PRISYM ID Extends 300x225 - PRISYM ID extends functionality of its flagship PRISYM 360 label lifecycle management solution for clinical trials and medical device organizations PRISYM ID extends functionality of its flagship PRISYM 360 label lifecycle management solution for clinical trials and medical device organizations Posted in: Clinical Trials, Medical Device, Press Releases, PRISYM 360 - The new modules recognise the constantly evolving operational and regulatory requirements life sciences and medical device organisations face. PRISYM ID…
PRISYM ID announces 300x225 - PRISYM ID Announces PRISYM SaaS PRISYM ID Announces PRISYM SaaS Posted in: Medical Device, Press Releases, PRISYM SaaS - Software-as-a-Service model enables SME medical device manufacturers to achieve rapid compliance and end-to-end label lifecycle management
A Surprise Package 300x225 - A Surprise Package A Surprise Package Posted in: Coverage - As global healthcare grapples with the problem of medication adherence, C Everett Koop’s famous observation has become a familiar retort:…
Compliant Labeling 300x225 - Compliant Labeling Inspection: Strategies for Success Compliant Labeling Inspection: Strategies for Success Posted in: Coverage - The continual tightening of regulation around the packaging and labeling of medical devices has so far failed to stimulate a…
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