Join industry experts from PRISYM ID to find out why data level inspection is vital to your labeling process.
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.
Many respondents experience frequent problems and blame human error.
Find out how Medical Device companies’ manufacturing practices may need to change due to social distancing guidelines.
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.
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.
Smiths Medical, Rolls-Royce and GKN Aerospace first to take ready-to-use solution.