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Prisym ID
Complying with labelling as EU MDR gets close
The labelling of medical devices can be a complex process. As EU MDR implementation heads closes, Mark Cusworth, Prisym ID asks - will your label comply? Read more
EU MDR: The nightmare before Christmas?
Mark Cusworth, PRISYM ID, examines EU Medical Device Regulation and its implications on labeling – and looks ahead to a Christmas future that could become a nightmare unless companies act now. Read more
Unique device identification: how do you get it right?
Warren Stacey of labelling specialist Prisym ID examines unique device identification implementation to date, and offers best practice guidance for compliance. Read more
