For EMI / EMC Engineers
The U.S. Food and Drug Administration (FDA) recently released a draft guidance document containing a list of recommendations for medical device companies who wish to claim electromagnetic compatibility (EMC) of products for premarket submissions.
The FDA will review these types of claims based on the risk of EMC malfunction or degradation of the device and in accordance with industry standards.
For more info, click here.
Established in 1970, Interference Technology helps EMI/EMC engineers find solutions to their various testing, design, application and regulatory issues by publishing articles, news and other practical content. We help suppliers in these areas to find the right customers for their components, materials, test equipment and services through a wide range of marketing services, including lead generation, branding, market research and events. The publication is available in various printed and electronic media formats, with readers in over 60 countries. We also publish issues in local languages in China, Japan and Europe.
