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.
Updates will help to streamline label and booklet production for adaptive clinical studies.
Five key points that will help you to understand the new GS1 Clinical Trial barcodes standards in more detail.
A Webinar from the Experts at KPMG & PRISYM ID on Meeting the Updated Timelines for EU MDR.
Discover how PRISYM ID helped to support Smiths Medical, Rolls-Royce and GKN respond to urgent demand for ventilators to combat Covid-19.
Due to Covid-19, on 17th April 2020, the European Parliament gave Medical Device companies a 12-month reprieve on EU MDR.
Smiths Medical, Rolls-Royce and GKN Aerospace first to take ready-to-use solution.
PRISYM 360 SaaS Labeling Solution Offers an Instant Validated Platform for COVID-19 Clinical Trials.
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.
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).