Siemens Digital Industries Software Blog Network

Siemens Digital Industries Software Blogs


Verification Horizons

Accellera’s DAC Breakfast & Panel Discussion

UVM: Charting the New Territory At this year’s DAC, Accellera introduces UVM (Universal Verification Methodology) to the world at its...

Corporate Blog

CAD folks, help me out with a simple survey experiment

PLM Connection is coming up and I’ve got a few more presentations and hands-on that last year. Like any of you, I’d like to present the right information so I’m thinking about the best mixture of con...

Embedded Software

Static or static

In English, the word “static” has a variety of meanings, but they can be summed up by the definition of...

Verification Horizons

Easier UVM Testbench Construction – UVM Sequence Layering

UVM Layering Package updated from OVM Layering Package In an earlier blog post, I discussed a sequence layering technique that...

Embedded Software

A good day out

Last Saturday, we had an interesting day out. It all started because Libby’s mother was going to the US and...

Corporate Blog

Avatars @ Ford

Avatars assemble vehicles at Ford? Yes they do! Virtual vehicles, of course, and the avatars are called Jack and Jill. In a recent article for Bloomberg Businessweek, Nick Barbe...

Corporate Blog

NX7 Part 4 – Lifecycle Simulation (CAE)

This is the 4th post on the new items in NX7.  In today’s post, I will review CAE or Lifecycle Simulation. NX 7.5 offers major enhancements across the entire CAE portfolio.  Some of the ...

Corporate Blog

HD-PLM Technology Framework Launched at Expo 2010 Shanghai China

As I previously mentioned, Siemens PLM Software launched its HD-PLM Technology Framework at Expo 2010 Shanghai China with a press event and product demonstrations. This was an ideal venue for address...

Polarion

Polarion Customers achieve FDA CFR 21 Part 11 compliance

Image: flickr The US Food and Drug Administration (FDA) is similar to many organizations embracing software to automate while forced to maintain legacy processes. FDA ruling 21 CFR Part 11 specif...