Date & Time
Jun 30, 2020 11:00am ECT
Before marketing of electric or electronic medical devices each manufacturer should conduct a risk analysis. If conducted correctly, the analysis will become useful and will support the manufacturer in the control of product related risks. Otherwise, it will be an unpleasant duty - a task which will swallow up company resources in vain and slow down the process of launching the product on the market.
This webinar focuses on main differences between 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.