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Understanding how ISO 10993-17 and ISO 10993-18 connect - WHITEPAPER
This whitepaper explores parts 17 and 18 of ISO 10993, how they relate, and considerations for industry.
Comparing EU and FDA approaches to regulating MedTech software and AI - WHITEPAPER
This whitepaper explores the different EU and FDA approaches to regulating MedTech software and AI.
MedTech 2020 Survey: EU MDR and IVDR Compliance
Complete our MedTech survey on EU MDR and IVDR Compliance to be in with a chance of winning a 2 day conference pass to MedTech Summit.