Articles Tagged with ''manufacturing''

Kassow Robots announced its Sensitive Arm technology across its complete range of 7-axis collaborative robots.

NEOTech, a premier provider of electronic manufacturing services (EMS), integrated design engineering, and advanced supply chain solutions for the aerospace and defense, medical device, and high-tech industrial markets, announced that its Agave 1 manufacturing facility in Juarez, Mexico, has officially received AS9100 certification.

Quality speaks with Eddie Pompa, a legend in the NDT industry. He's an NDT advocate and educator and mentor to many in the field.

Material fatigue is a critical concern in engineering, with over 90% of failures caused by fatigue stress rather than overloading. As industries push material limits, efficient fatigue testing becomes vital. Rotating beam fatigue testing, dating back to the mid-1800s, provides a cost-effective way for researchers to evaluate material endurance while saving time and money.

There are record levels of uncertainty today, but Taylor St. Germain of ITR Economics says strong growth is ahead. He says manufacturers should follow the data—not just the headlines—and be prepared for growth for the next few years. Listen for his advice and insights regarding rising costs, labor challenges, and tariffs.

Advantive, a mission-critical software provider for specialty manufacturing and distribution businesses, announced its acquisition of PINpoint, a manufacturing execution system (MES) based in Burlington, Ontario, Canada.

This article highlights some key points of product hazard analysis.

e-con Systems® introduced the ONVIF-compliant 4K HDR GigE Camera - RouteCAM_CU86 - built with the Sony STARVIS 2 IMX678 sensor and engineered to provide exceptional image clarity and reliability even in the most challenging lighting environments.

Kitov AI announced the availability of Kitov AI 2.9, a significant update to its acclaimed software platform.

This article explains how a Quality leader can establish external requirements by defining products in a specific region, using medical devices as an example based on FDA regulation Section 201(h) and the 513g Request process. Following this prevents wasting time, funds, and resources on incorrect regulatory assumptions.