A Webinar from the Experts at KPMG & PRISYM ID on Meeting the Updated Timelines for EU MDR.
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Discover how PRISYM ID helped to support Smiths Medical, Rolls-Royce and GKN respond to urgent demand for ventilators to combat Covid-19.
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Posted in Achieving Regulatory Compliance , Assisting With The Consolidation , Business Analysis , Case Study , Enabling the Expansion , Increasing The Operational Efficiency , Information Technology , Medical Device , Operations & Labeling , Overcoming The Technical Challenges , Project Managers , Reducing Risks , Regulatory & Compliance Smiths Medical, Rolls-Royce and GKN Aerospace first to take ready-to-use solution.
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PRISYM 360 SaaS Labeling Solution Offers an Instant Validated Platform for COVID-19 Clinical Trials.
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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.
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With the EU confirming the postponement of EU MDR to May 26th 2021, the medical device industry has time to get its house in order. Read More
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).
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Join medical device labeling and data experts from PRISYM ID and Reed Tech to find out the best practices for UDI Data & Product Labeling.
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PRISYM ID introduces an InDesign Plugin to its life science dedicated label and artwork management platform, PRISYM 360.
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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.
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