Webinar
Medical Devices

Navigating the Complex IVDR Landscape

This webinar presents an overview of the key aspects of IVDR compliance, focusing on technical documentation and Performance Evaluation.

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This webinar:

Clear IVDR requirements to you .
Significant Changes under Article 110.
Key issues identified during IVDR application to a Notified Body.
Technical Documentation.

Speakers

Hear from the experts in this webinar

Speaker

Elizabeth Harrison

Global Head - IVD, BSI

Insights & Media

Find out more from global experts in healthcare standards

Informatie en media

EU MDR – Post Market Clinical Follow-Up

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Annex XVI - Devices Without an Intended Medical Purpose

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Using Standards to Demonstrate Conformity

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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Symbols & Details Required for Medical Devices & IVDs

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