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Thought and Commentary for the Medical Device Industry

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2020s Predictions: Get Ready for More Regulations

January 13, 2020 | Posted by JAMA
Velentium was pleased to contribute to this blog series from JAMA Software, which solicited input from thought leaders across industries to forecast what's next for medical device development and...

5 Additional Benefits Your UDI Could Be Providing

September 26, 2019 | Posted by Devin Carroll
You have been working hard to place Unique Device Identification (UDI) numbers on each of your devices. You now know more about bar codes, QR codes, scanner systems, and federal databases than you...

Static Analysis (Part 4): Configuring Parasoft for Secure Development

July 29, 2019 | Posted by Satyajit Ketkar
Welcome back to our final installment of the series on Static & Dynamic Analysis, including Unit Testing. This last blog post will focus on the basics of the Parasoft testing tool, as well as provide...

Quality Systems (Part 6): Four Goals of a Valuable QMS

July 1, 2019 | Posted by Randy Armstrong
The principal objective of a QMS for a medical device company is patient safety. Patient safety is well understood and communicated throughout the medical device industry, leading to an almost...

Quality Systems (Part 5): Simple is Hard, but Simple is Worth it

June 24, 2019 | Posted by Randy Armstrong
In the second blog post in this series, we explained that a lean QMS results in less complicated devices, which in turn decreases development time, cost, and, in many cases, patient risk. Less is...

Quality Systems (Part 4): Standards-centric vs. Product-centric

June 17, 2019 | Posted by Randy Armstrong
In the 4th part of this series, we are going to talk about the differences between a QMS that is standards-centric and one that is product-centric.

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