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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The Second-Annual JamaCon Draws Global Customers, Valued Partners, and Industry-Leading Experts
With over 50 companies representing 13 countries, the collective knowledge and experience present in the room at JamaCon 2019 was incredible.
Webinar Extra: More Answers About Effective Requirements Reviews
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.
When Jira® and Confluence® Are Not Enough for Complex Product Development
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.
2020s Predictions: Get Ready for More Regulations
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.
Scaling Up Agile Teams: How Enterprise Companies Can Remain Competitive in a Startup Market
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.
Industry Roundup: Medical Device Technology Advances in the Wake of Cybersecurity Concerns
Despite ongoing concerns about cybersecurity, the medical device landscape has seen some amazing advances even just this year.
The Importance of ISO 26262 in Automotive Development
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.
5 Ways to Build a Safety-First Culture
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.
How the FDA’s New Safety and Performance Based Pathway Could Affect Medical Device Development
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.