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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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Velentium Lineup of Speakers Set at MD&M West

January 24, 2023 | Posted by Lindsey Dinneen
MD&M West will feature an array of speakers from Velentium experts in the technology, product security and human factor spaces 

Velentium Directors to Speak at MD&M Minneapolis

October 26, 2022 | Posted by Lindsey Dinneen
Albert Rodriguez to present on user-centered design for MedTech devices and Christopher Gates to host a presentation on aligning FDA expectations and EU’s MDR regulations for cybersecurity

Webinar Oct. 6: Applying IEC 62304 Principles to Electrical and Mechanical in Medical Device Design

September 27, 2022 | Posted by Lindsey Dinneen
Velentium is pleased to partner with Greenlight Guru to present a free live webinar, “Extending IEC 62304’s Software Lifecycle Principles to Electrical and Mechanical in Medical Device Design,” with...

Case Study: Building a Partner Ecosystem to Win the Fight Against Opioid Withdrawal

March 9, 2022 | Posted by Lindsey Dinneen
Effective Opioid Response In the yearlong period ending April 2021, over 100,000 Americans died from drug overdose, the vast majority from synthetic opioids. An estimated 4 million of the 11 million...

Closing the Software Loophole: How to Mitigate Cybersecurity Vulnerabilities in Medical Devices

February 17, 2021 | Posted by Jason Smith
Is your team prepared for cybersecurity threats and the evolving focus from the FDA? Most medical device manufacturers and software teams find this topic uncomfortable - and rightly so. Many of us...

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...
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