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Thought and Commentary for the Medical Device Industry

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Health Sector Coordinating Council’s Recommendations for Enhanced MedTech Cybersecurity Receives Further Industry Endorsement

April 19, 2022 | Posted by Lindsey Dinneen
Velentium’s Director of Product Security helped draft industry standard

Understanding the Cybersecure Development Lifecycle

September 14, 2020 | Posted by Chris Gates

Executing Successful Design Reviews Part III - Final Tips

March 2, 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...

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)....

Design for Manufacturing Part II - Scenario A

February 4, 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...

2020s Predictions: Medical Device Security and Accountability

January 20, 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...

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