Question: How should we proceed with respect to the Canadian certification for our wireless device following changes we’ve made to it?...

The FCC no longer accepts a “manufacturer’s declaration of gain” without any supporting justification. At a minimum, each Part 15...

The European Parliament and the Council of the European Union adopted Regulation (EU) 2023/1542, a new regulation on batteries and waste...

Personnel changes require that we update the contact information for our FCC Grantee Code that was registered many years ago. What do we...

What is the deadline for adding the UKCA mark to our wireless products destined for the United Kingdom? At this time, there is no longer...

Question: We want to FCC certify a new line of wireless modules that cannot be tested in a stand-alone configuration. How should we...

When designing PCBs, various ways exist to achieve copper balancing and prevent warping during automated soldering. One common method is...

On January 31, 2020, the United Kingdom left the European Union. And in May of 2020, the European Union will introduce the new EU MDR ...

Does your company manufacture or market medical devices in the European Union? Then you’re probably aware of the upcoming implementation ...

The European Union’s Radio Equipment Directive (RED), which delineates essential requirements for all radio equipment marketed in the EU,...

In the past several years, many changes have been made to the regulations and rules governing the medical device industry—and there are ...