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 ...
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 ...
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