MattMantraSystems
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The webinar helps you to get beneath the skin of the EU MDR and understand the key requirements for medical device regulatory compliance. It will also help you build active regulatory systems that will safeguard your MDR transition through targeted knowledge and understanding. Learn the secrets to generating, identifying, appraising and analysing clinical evidence for medical device compliance. And access powerful resources and personal support that will complement your internal capabilities in working with the MDR.
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