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Mock EU Notified Body Audit

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Mock EU Notified Body Audit

If your medical device is in any other class apart from class I, you will have to provide the Notified body with proof that your product fulfils the essential requirements of the respective CE directives. The medical devices of Class III hold the highest risk.

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MOCK EU NOTIFIED BODY AUDIT
MOCK EU NOTIFIED BODY AUDIT

Bridgemed Solutions consultant helped the organization establish checks and balances, as well as identify and handle potential audit findings from the notified authority.  


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