To streamline the oversight of manufacturers’ quality systems, and encourage improved product safety on a global scale, the International Medical Device Regulators Forum (IMDRF) has developed the Medical Device Single Audit Program (MDSAP).
The CE marking is also called a “product’s passport” for the markets within the European Economic Area (EU Member States plus Liechtenstein, Iceland and Norway) and in Turkey. It is the first indication that a product complies with the requirements under European Product Law.
Why the effects of nearby lightning might be over-estimated, or in some cases underestimated, and how to get more realistic estimates.
This s-parameters tutorial consists of two parts: Part I discusses the fundamental background needed to understand the concept of s-parameters; Part II explains the s-parameters use in EMC measurements and testing
S-parameters are very useful to evaluate, understand, and optimize the response of your filters. If you are unfamiliar with this typical tool for RF engineers, this column is for you.
How does a standard become the “Standard”?
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