Join industry experts from PRISYM ID to find out why data level inspection is vital to your labeling process.
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Posted in Achieving Regulatory Compliance , Business Analysis , Clinical Trials , Increasing The Operational Efficiency , Information Technology , Medical Device , Operations & Labeling , Overcoming The Technical Challenges , Pharmaceuticals , Project Managers , Supply Chain , Webinar
PRISYM ID are delighted to be attending the Clinical Trial Supply Forum virtual event on August 25-26th 2020.
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Five key points that will aid better understanding of EU MDR labeling following the year extension to regulation implementation. Read More
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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