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FDA Warns Against Unauthorized Modifications to Medical Devices

The U.S. Food and Drug Administration (FDA) is also stepping up its efforts to identify FDA-cleared medical devices that have been subsequently modified and that no longer fall within the scope of their original clearance.

ESD Testing Parameters

Navigating the complex world of ESD testing standards? This blog examines how discharge parameters vary across standards, from aerospace's CS118 to automotive's ISO 10605. Discover how resistance and capacitance values affect test severity and learn when to apply custom parameters for your specific threat environment.

FDA Alerts the Medical Device Industry About Unreliable Third-Party Test Data

The U.S. Food and Drug Administration (FDA) is advising medical device manufacturers to take steps to verify the accuracy and reliability of third-party testing data before submitting it to the FDA.

FCC to Investigate CCP-Aligned Entities

The U.S. Federal Communications Commission (FCC) has launched a major investigation into entities operating in the U.S. that are aligned with China’s Communist Party (CCP) and whose communications equipment has been placed on the FCC’s Covered List.

Designing for EMC Compliance in Consumer Electronics

This practical guide explores the critical challenges of electromagnetic compatibility in modern consumer electronics, from smartphones to wearables. Learn key design strategies for managing interference in increasingly compact devices with real-world examples. 
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NIST Releases Draft of Quick Start Guide for Cybersecurity Framework 2.0

The U.S. National Institute of Standards and Technology (NIST) has released for public comment a draft of a Quick Start Guide for its Cybersecurity Framework 2.0.

Was it the Radar? Respectfully Revisiting the 1967 US Navy USS Forrestal Carrier Disaster: Part 2

How can the EMI/EMC community continue to blame this accident on electromagnetic interference (EMI) from the USS Forrestal’s on-board AN-SPS-43 search radar when the official US Navy inquiry comes to different conclusions?

EU Commission Releases Its Consumer Conditions Scoreboard

The Commission of the European Union (EU) has published its biennial report monitoring consumer sentiment across the EU in connection with consumer conditions in the Union.

Achieving and Sustaining Medical Device Compliance

Change is the only constant. A product lifecycle approach underpinned by a proactive and reactive regulatory and compliance strategy is key to success. Using digital tools to augment that process generates faster yet reliable data and results to bring safer medical devices to market that improve patient outcomes.

Filter Designs for Switched Power Converters: Part 2

This series of articles delves into the design principles of power filters for switched-mode power converters and similar applications, focusing on conducted and radiated emissions. Part 2 will examine specific aspects of switched power converters.
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