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That is a great post. I quoted it in the post if that is cool and will read up on some those references. Do you think that a lot of that complexity would be re
by grahar64 11y ago
That is a great post. I quoted it in the post if that is cool and will read up on some those references.
Do you think that a lot of that complexity would be reduced by opening it up to a wider development community through open source? How much open source, consumer electronics, were used? Did you source the transducers from another company, or make them in house?
Cheers again for the comment.
- jes 11y agoThank you for your kind words. The post is necessarily incomplete; I don't think I can give you a full appreciation for all that is involved. And I don't wish to give the impression that ultrasound is necessarily more complex than other imaging modalities, such as MRI, PET, etc. I wouldn't rule out open source, and many open source tools are used in the engineering process (e.g., gcc, git, etc.) I don't know about including open source components in a commercial code base, though. The lawyers usually ran away screaming whenever we would suggest using any open-source code. Certainly the high-volume electronics industry makes components that are used in ultrasound systems. Some of the ARM SOCs, for example, and I suppose, some of the FPGAs, DSPs, etc. There are also a number of custom components, such as ASICs and combined analog-digital parts that show up in the so-called "front end." The companies I have worked for designed their own transducers. That really is a science as well. Making a transducer probably involves at least 100 - 150 process steps, and some very expensive equipment (dicing saws, for example.) You also often have injection-molded parts (e.g., the transducer handle itself) that are expensive to produce (the molds for the injection molding machine are done with 3D solid modeling tools, then CNC machined from steel, etc. You also have whole departments of people that work in "Regulatory Affairs" and/or "Compliance Engineering." You also need to employ people to "optimize" your ultrasound images, in each of the different modes you might support: B-mode (2D), doppler, M-mode, color power doppler, etc. You also have things like harmonic imaging, etc. Then there is sending images you have collected off to the various PACS systems that hospitals have. This usually involves a complex protocol known as DICOM. Ok, I'm out of gas for this comment. Again, not trying to drown you in jargon, just suggesting that there is a reason that new ultrasound machines tend to be pricey; that reason is that NRE (non-recurring engineering) is very expensive, actually building the boards is expensive, shipping the systems and maintaining them in the field is expensive, and maintaining all of the other systems you have to have in place to be a viable ultrasound company is really expensive. Hope this helps; thanks for letting me share a bit of my experience.
- bronson 11y agoOne more warning... Two years ago I was on a project that spec'd inexpensive transducers from China. We bought samples from multiple factories and they were all terrible. Datasheets were vague, and a lot of the transducers didn't even meet those weak specs. Ultimately it didn't matter much for our beauty product but it would be a big problem if we tried to use them for imaging.
- HeyLaughingBoy 11y agoYup. Yet one more cost: Supply Chain control is vital.
- jes 11y agoAgain, valid point. At one point in time, I had a number of people in incoming receiving working for me. We had to do all kinds of quality control on incoming components, such as castings, PCBs, etc. We had automated measuring machines, etc. It's all very expensive to set this stuff up and staff it. We also had to use an XRF gun on parts, to make sure we weren't being shipped non-RoHS parts. As I remember, one of the add-ins for our Agile PLM system (Agile is an Oracle product) was on the order of a few hundred thousand dollars for licensing fees and setup, not counting the months of consulting time necessary to load bills of materials, etc., into the system.
- HeyLaughingBoy 11y agoOn the topic of Open Source, our IP attorney was primarily concerned with licensing, but that's because he's an IP lawyer. Our Regulatory and Quality Assurance people would be far, far more concerned with the Design History of any open source code we tried to bring into a medical device product. How was it developed? Where are the requirements? How was the output validated against the requirements? Our process mandates Design and Code inspections, can we show that they were performed on this Open Source product, etc, etc, etc. Once you see the uphill road, you realize you're better off starting from scratch and writing the product yourself instead of depending on OSS. For some noncritical aspects, it's fine, but then you get into the definition of "noncritical" :-)