Questions from Notified Bodies: how to answer them?

In the context of regulatory compliance and medical devices certification, a Notified Body assessment is not only a requirement but a crucial aspect of ensuring the safety and quality of medical devices.

Whether it's during the conformity assessment process, audits, or post-market surveillance, these assessments may require additional information to be provided by the Manufacturers. These inquiries often demand meticulous responses that can significantly impact product approval timelines and market access.

This webinar is tailored to provide insights and practical strategies for effectively addressing questions from Notified Bodies.