PRISYM ID makes new senior appointment in clinical trials arena .
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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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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
PRISYM 360 SaaS Labeling Solution Offers an Instant Validated Platform for COVID-19 Clinical Trials.
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Former CEO and CFO join non-executive board and announce Richard Adams and Lauren Patterson to key executive positions.
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PRISYM ID has been identified as the UK’s best-performing scale-up technology company in the government and healthcare software category.
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