In this chapter, I will present a few useful “cookbook” applications for real-time control circuits designed to perform some specific low-level task and interface with a master controller for ...

If you are developing a medical device for the U.S. market, you first need to determine how your device will be classified by FDA. If you do not know the FDA classification, I recommend you go check ...

Bioprocessing is an umbrella term that describes the research, development, manufacturing, and commercialization of products derived from or used by biological systems. For industrial purposes, ...

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 ...

Today's SoCs include hundreds of complex IP blocks with millions of transistors each. CSRs are essential for managing these IPs, with some systems having up to a million CSRs. IP-XACT standards help ...

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 ...

Identifying constraints explicitly in the design-input document facilitates project management and reduces risk. by Gerald E. Loeb and Frances J. R. Richmond Figure 2. Display window containing ...

The course consists of three weeks of materials and is focused on modeling and control of grid-tied power electronics. Upon completion of the course, you will be able to understand, analyze, model, ...

How to read Bode plots to assess dynamic control behavior of a power-supply design. Observing Bode plots from an example voltage regulator to observe control-loop speed and stability. This article ...