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Improving Lives for a Better World, One Device at a Time

Thought and Commentary for the Medical Device Industry

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Executing Successful Design Reviews Part II - Conducting Successful Reviews

February 27, 2020 | Posted by JAMA
This blog series is jointly based on the expertise of Randy Armstrong, Chief Technology Officer at Velentium, and Jama Software’s experience working with developers of Class II and III medical...

Executing Successful Design Reviews Part I - Creating a Review-Positive Culture

February 25, 2020 | Posted by JAMA
This blog series is jointly based on the expertise of Randy Armstrong, Chief Technology Officer at Velentium, and Jama Software’s experience working with developers of Class II and III medical...

Book Review - What You Do is Who You Are

February 21, 2020 | Posted by Velentium Book Club
About once a quarter, Velentium offers its staff the opportunity to read & discuss a business-related book together. It’s a chance for us to take a break from chopping firewood and sharpen our...

Design for Manufacturing Part V - Pros and Cons

February 18, 2020 | Posted by Devin Carroll
Velentium offers a selection of services that represents the entire lifecycle of a device. Our engineers, developers, SMEs, manufacturing technicians, and production managers who support those...

Design for Manufacturing Part IV - Scenario B

February 14, 2020 | Posted by Devin Carroll
Velentium offers a selection of services that represents the entire lifecycle of a device. Our engineers, developers, SMEs, manufacturing technicians, and production managers who support those...

How Medical Device Developers Can Prepare for EU MDR

February 11, 2020 | Posted by JAMA
The following is an edited transcript of JAMA Software's interview with Sat Ketkar, Principal System Architect & Engineer here at Velentium, regarding the EU's new Medical Device Regulation (MDR)....
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