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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 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

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...

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...
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