Medical device companies that identify quality problems early on can prevent product development costs from spiraling out of control, while also laying the groundwork for design verification and ...

The dynamic world of compliance is continually evolving. New regulations, emerging technologies, and changing market conditions demand that organizations remain vigilant and proactive in their ...

Multivariable control systems design addresses the challenges of controlling processes with several interacting inputs and outputs. This field synthesises advanced control theories with practical ...

Both software and hardware are parts of all motor control systems such as IGBTs, WBG semiconductors and MCUs. Industry 4.0 strongly relies on motor control for its development but energy consumption ...

RAPS.org needs your explicit consent to store browser cookies. If you don't allow cookies, you may not be able to use certain features of the web site such as ...

Interactive configurators, real-time data access, RFQ automation, expert-guided product selection and error prevention are ...

FDA's quality system regulation (QSR) is often perceived by medical product developers as unnecessary overhead. Software developers, in particular, often see it as a nuisance that delays the ...

When striving for long-term sustainability, designers have latitude as to how complex a system they wish to design. Build sustainability into every aspect of the control panel’s life—design, ...

Control Design helps original equipment manufacturers (OEMs)-machine builders, system integrators and engineering firms-to master the use of controls and automation in designing and building equipment ...