2020s Predictions: MBSE and the Digital Thread
In the second installment of our 2020s Predictions series, we’re featuring predictions from Dirk Zwemer, President at Intercax, a global innovator in the field of model-based systems engineering (MBSE).
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In the second installment of our 2020s Predictions series, we’re featuring predictions from Dirk Zwemer, President at Intercax, a global innovator in the field of model-based systems engineering (MBSE).
With over 50 companies representing 13 countries, the collective knowledge and experience present in the room at JamaCon 2019 was incredible.
Ahead of our recent webinar, “Ask Jama: Tips and Tricks for More Effective Reviews,” we asked those who registered to quiz us with their toughest queries around reviewing requirements.
To meet quality demands in complex product development and improve speed to market, development teams are focusing on improving one of the most vital steps in their process: requirements management.
Thoughts on the decade ahead from Josh Turpen, Chief Product Officer at Jama Software, who oversees the ongoing innovation and refinement of our core product offerings.
In this blog post, we examine several different companies that have implemented Agile methods successfully and review what worked, what didn’t, and how companies can launch Agile teams that work.
Despite ongoing concerns about cybersecurity, the medical device landscape has seen some amazing advances even just this year.
When teams aren’t set up with the right tools, implementation strategies, and best practices, compliance with ISO 26262 becomes an afterthought — and an auditing nightmare.
Today’s move-fast-get-it-to-market-yesterday product development culture puts a lot of pressure on companies to innovate quickly, but creating a safety-first culture can save you from product recalls and failure.
The US Food and Drug Administration (FDA) has issued new guidance that expands the Abbreviated 510(k) Program for medical device development and premarket notification submissions.