Updated EU Guidance Reinforces How Notified Bodies Should Use Existing Evidence

Notified bodies’ conformity assessment processes can easily be streamlined and made potentially less costly within the context of the EU’s current regulations.

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Looking Back May Speed Up The Onward Regulatory Journey • Source: Shutterstock

During their structured dialog in the pre-application phase, manufacturers and notified bodies should agree on which evidence from previous applications can be reused.

This clarification is featured in a new answer contained in the Medical Device Coordination Group’s just-released fifth revision of its...

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