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

Thought and Commentary for the Medical Device Industry

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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...

Utilizing MC Squared Webinar: HSCC's Model Contract Language for MedTech Cybersecurity

July 22, 2022 | Posted by Jason Smith
Increasing cybersecurity threats are a major challenge facing healthcare companies, from hospitals to research facilities to medical device manufacturers (MDMs). To date, dialog between various...

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)....

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