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Ilo Classification PDF Overview Form

Ilo Classification PDF Overview Form

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today we're talking about classification with aduco life sciences trainer richard young hello everybody welcome to this session richard could you give us a bit of an overview of um classification regulations and requirements um under the new mdr for devices yeah certainly classification of product classification in europe there's no it's not a new thing it's something we've had in medical devices since the original medical device directive came out in the early 90s uh and you know the basic tenet of it is that some products are inherently more risky than others and we should spend more time designing and manufacturing those well than we did on on lower risk classification products so risk classification is a series of rules that allow us to assign a risk to a product based on those factors and and give us some guidance to how we're going to develop the product and how the conformity assessment is going to be conducted for it yeah so richa

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