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If you intend to become a medical device supplier or sub-contractor, you need to be aware of the different medical device regulations in the regions or territories you intend to conduct business in. Here are some quick guides to help you get started.
A guide to the medical device regulation (MDR) and the in vitro diagnostic device regulation (IVDR) was recently published. Here's what you need to know.
Medical device classifications can vary between the US and the EU. See some important examples here.
See how medical device regulations (MDR) vary in the UK and the EU and how they can affect medical device suppliers and manufacturers.
