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171Blog Post

Rimac Nevera Receives US Homologation and Green Light For Deliveries

Jama Software is always on the lookout for news on our customers that would benefit and inform our industry partners. As such, we’ve curated a series of customer spotlight articles that we found insightful. In this blog post, we share content, sourced from InsideEVs, about one of our customers, Rimac Nevera titled “Rimac Nevera Receives […]

173Blog Post

Considering DOORS® for requirements management? There is a more modern solution.

Considering DOORS® for requirements management? There is a more modern solution. If you’re considering IBM® DOORS® for requirements management, it might be because it’s considered a “safe” move, you’ve used it in the past, or because you’re unaware that there’s a significantly more modern and easier to use alternative to DOORS requirements management. IBM DOORS […]

174Blog Post

Best Practices for Efficient and Compliant Risk Traceability from Design to Manufacturing

Best Practices for Efficient and Compliant Risk Traceability from Design to Manufacturing Intro Those familiar with medical device development know that risk traceability and risk management is an important aspect that threads through the entire product development process and lifecycle. Many see risk management as discrete deliverables completed by different team members at certain phases […]

175Blog Post

What is DOORS® and Why Does DOORS® Software Fall Short for Requirements Management?

What does DOORS® stand for? DOORS is an acronym that stands for Rational Dynamic Object Oriented Requirements System. What is DOORS? IBM DOORS, formerly known as Telelogic DOORS, is a legacy requirements management tool originally created in 1991 and is part of the IBM Engineering Requirements Management DOORS Family. Why was IBM ® DOORS ® […]

176Blog Post

[Webinar Recap] Understanding Integrated Risk Management For Medical Device

In this blog, we recap the “Understanding Integrated Risk Management for Medical Device” webinar. Companies involved in developing medical devices understand the importance of risk management, but their approaches can vary significantly in terms of the time it takes to manage risk, the ability to connect risks to specific requirements and tests, and the capacity […]

178Blog Post

G2 Again Names Jama Connect® the Leader in Requirements Management Software

G2 Again Names Jama Connect® the Leader in Requirements Management Software Thank You to Our Customers! Jama Connect® was once again named the leader in the Summer 2022 G2 Grid® Report for Requirements Management Software! In addition to the honor of being named the only leader in requirements management software, we are proud to showcase that […]

179Blog Post

Notable Changes in the New FDA Draft Guidance – Content of Premarket Submissions for Device Software Functions

Notable Changes in the new FDA Draft Guidance – Content of Premarket Submissions for Device Software Functions The FDA released its new draft guidance for the Content of Premarket Submissions for Device Software Functions on November 4, 2021. Once approved, this guidance will replace the preexisting Guidance for the Content of Premarket Submissions for Software […]

180Blog Post

[Webinar Recap] Managing Mission Critical Requirements in an Agile Environment

In this blog, we recap the “Managing Mission Critical Requirements in an Agile Environment” webinar. Over the last two decades, Agile has been demonstrated to be a powerful approach to software and systems development. It has taken on a number of representations but there are features that most representations share – namely “flexibility” when dealing […]