Accelerate Medical Device Development with Modern Requirements Management
3 improvement strategies to insert risk control as a crucial part of the medical device development framework to comply with ISO standards and EU MDR.
3 improvement strategies to insert risk control as a crucial part of the medical device development framework to comply with ISO standards and EU MDR.
Traceability makes it possible to manage and respond to change in a systematic, auditable, confidence-enhancing way in complex product development.
From Berlin to Munich, product development teams in Germany are wrestling with a familiar question: How do you balance efficiency and quality as the scope of your projects grows increasingly complex?
LDRA’s technical product manager talks predictions on a continued trend in the embracing of test automation and the use of artificial intelligence.
In the fourth installment of our 2020s Predictions series, we’re featuring predictions from Robin Calhoun, Senior Product Manager at Jama Software, as well as a certified Scrum Master.
Rimac Automobili’s innovation and success have supercharged its growth. To manage its rapidly-growing, complex large-scale systems for automotive development, the pioneering company turned to Jama Connect.
In the third installment of our 2020s Predictions series, we’re featuring medical device security predictions from Chris Gates, Principal Systems Security Architect at Velentium, a professional engineering firm specializing in the design and manufacturing of therapeutic and diagnostic active medical devices.
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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