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
Changing regulations, such as Annex VI clinical trial regulation, need to be incorporated into the label and artwork processes in time for when the regulation takes effect.
PRISYM ID will be attending this years RAPS Regulatory Convergence on September, 22-24 2019 in Philadelphia.
PRISYM ID will be presenting at this year’s MedTech Intelligence, Virtual Conference on 23rd and 24th May 2019.