Many respondents experience frequent problems and blame human error.
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PRISYM ID will host its first-ever virtual stand at a prestigious industry event which has gone digital this year in response to the COVID-19 pandemic.
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Updates will help to streamline label and booklet production for adaptive clinical studies.
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Five key points that will help you to understand the new GS1 Clinical Trial barcodes standards in more detail. Read More
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
Due to Covid-19, on 17th April 2020, the European Parliament gave Medical Device companies a 12-month reprieve on EU MDR.
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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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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
