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FDA Warns Manufacturers to Scrutinize Third-Party Testing Data

The U.S. Food and Drug Administration (FDA) is reminding medical device manufacturers to independently verify testing results generated by third parties that are included in premarket submissions to the agency. In a Letter to Industry...

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EMC & eMobility

For a company embarking on EMC testing for either component or vehicle-level testing of their EV products, it is necessary first to have a good understanding of the EMC regulatory situation. Although some of the EMC testing of EVs remains identical to that of their combustion engine equivalents, additional testing of EV motors, EV batteries, and EV charging stations is now required. Existing EMC facilities may need to be upgraded or new ones specifically designed to carry out such tests, and this white paper will take the reader through the details of these needs.

FCC Adopts Rules to Enable Consumers to Stop Robocalls, Robotexts

As part of its ongoing effort to stem the rise in unwanted robocalls and robotexts, the U.S. Federal Communications...

EU Commission Issues Regulations for Cybersecurity Certification Scheme (EUCC)

The Commission of the European Union (EU) has published detailed regulations for the cybersecurity certification of certain products, taking...

A Dash of Maxwell’s: A Maxwell’s Equations Primer – Part Two

Maxwell’s Equations are eloquently simple yet excruciatingly complex.

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FDA Amends Quality System Regulations for Medical Devices

In an effort to stay current with new and updated international standards, the U.S. Food and Drug Administration (FDA)...

U.S. and EU Sign Joint Cybersafe Products Action Plan

The U.S. and the European Union have signed an agreement to work collaboratively to strengthen the cybersecurity of Internet-of-things (IoT)-capable hardware and software products used by consumers.

FCC Makes AI-Generated Robocalls Illegal

In a landmark decision, the U.S. Federal Communications Commission (FCC) has unanimously ruled that robocalls made with voices generated by artificial intelligence (AI) tools are illegal.

EU Commission Proposes More Time for Compliance with In Vitro Diagnostics Regulation

The EU Commission has proposed providing manufacturers of certain medical devices with additional time to comply with the requirements of the EU’s IVDR.

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Discover new products, review technical whitepapers, read the latest compliance news, trending engineering news, and weekly recall alerts.