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.
Krzysztof Wasilewski is a Senior Project Engineer at UL with vast experience in certifying various types of laboratory and medical equipment.
June 30, 2020