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  • On-demand Webinar

Things to Know about ISO 14971 3rd Edition

Gain an understanding of the main differences between the 2nd edition and 3rd edition of ISO 14971.

Laptop on table beside stethoscope and medical chart

Before marketing electric or electronic medical devices, manufacturers should conduct a risk analysis. If conducted correctly, the analysis will become useful and will support manufacturers in the control of product related risks. Otherwise, it will be an unpleasant duty - a task which can swallow up company resources in vain and slow down the process of launching products to the market.

This webinar focuses on the main differences between the 2nd edition and 3rd edition of ISO 14971. Learn more about the new chapter structure, scope, terms and definitions.

 

Speaker

Krzysztof Wasilewski is a Senior Project Engineer at UL with vast experience in certifying various types of laboratory and medical equipment.

Webinar date

June 30, 2020

Updates: ISO 14971 3rd edition

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