February 11, 2022
In this article, Jeffery Nelson, Kate Corr, and Paul Huish discuss mask regulations, amended qualifications during COVID-19 and the rise of fraudulent products on today’s markets. Read Full Story
See BlogNovember 27, 2018
Medical devices marketed in the European Union are required to comply with a set of medical device directives called the “medical devices regulation” or MDR for their Conformité Européenne (CE) marking and marketing in Europe. Over the past decades, the...
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