PRISYM ID are delighted to be attending the Clinical Trial Supply Forum virtual event on August 25-26th 2020.
Five key points that will aid better understanding of EU MDR labeling following the year extension to regulation implementation.
Find out how Medical Device companies’ manufacturing practices may need to change due to social distancing guidelines.
Five key points that will help you to understand the new GS1 Clinical Trial barcodes standards in more detail.
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 ID will be exhibiting and hosting a workshop at this year’s American Medical Device Summit on October 28-29, 2019.
PRISYM ID will be exhibiting at the Clinical Trial Supply East Coast 2019 on the 16th and 17th of October, in King of Prussia, booth 16.
Here’s a blog about the new GS1 Standard for Clinical Trials and how we can help you adopt it