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- Mouser Electronics is an authorized global distributor of the newest products from Altera.
NGMN Urges Telcom Ecosystem to Take Lessons From 5G For 6G Simplification
According to two new Next Generation Mobile Networks Alliance (NGMN) industry publications, enabling the full potential of 6G requires a different standardisation approach to prevent complexity and market confusion, alongside a smooth and cost-effective migration path with a focus on MRSS as a baseline solution.MAHLE and Rohde & Schwarz Develop Application for Sensor Testing of Modern Driver Assistance Systems
The technology groups MAHLE and Rohde & Schwarz have jointly developed a technical application that can be used for the first time to reliably check sensors of modern driver assistance systems (ADAS) after a repair.Square Peg Communications and VIAVI Solutions Join Forces to Advance 5G NTN Testing
Square Peg Communications announced a strategic partnership with VIAVI Solutions to deliver advanced test capabilities for the rapidly emerging 5G NTN market.Vishay Intertechnology Extends ILHB Series of Automotive-Grade Ferrite Beads
Vishay Intertechnology, Inc. announced an expansion of its ILHB series of automotive-grade multilayer chip ferrite beads for high current filtering.FocalPoint’s Precise+ Enables Sub-Metre GNSS Accuracy in the Toughest Environments
Focal Point Positioning has announced Precise+, a new technology that delivers reliable high-precision positioning in tough environments where conventional carrier phase tracking fails.EMC Bench Notes: Interpreting Emissions Using a Near-Field Probe
Not all EMC emissions look alike — and knowing the difference can save your compliance test. Kenneth Wyatt breaks down how to use near-field probes to identify and interpret broadband versus narrowband emission profiles, so you can trace noise back to its source before it becomes a costly failure.
The post EMC Bench Notes: Interpreting Emissions Using a Near-Field Probe appeared first on In Compliance Magazine.
FDA Releases Guidance Document on Human Factors Information in Marketing Submissions
The FDA has finalized its guidance on human factors information required in medical device marketing submissions, outlining a risk-based framework for 510(k)s, PMAs, De Novo requests, and HDE applications. Here's what manufacturers need to know before their next premarket submission.
The post FDA Releases Guidance Document on Human Factors Information in Marketing Submissions appeared first on In Compliance Magazine.
FDA Updates List of Recognized Consensus Standards
The FDA has updated its list of more than 1,700 recognized voluntary consensus standards used to demonstrate compliance in medical device premarket submissions. Find out which specialties are covered and how declarations of conformity can streamline your path to market authorization.
The post FDA Updates List of Recognized Consensus Standards appeared first on In Compliance Magazine.
Remcom Highlights Five Real-World Applications of its EM Simulation Technologies
Remcom is highlighting 5 major use cases of its electromagnetic (EM) simulation technologies at the ongoing IMS 2026, in Boston, Massachusetts. IMS 2026 (IEEE MTT-S International Microwave Symposium)..