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A comprehensive look at ISO/IEC/IEEE 15288 goals, standards, and tools to achieve compliance. Product development is evolving quickly; over the past few years, it’s become increasingly complex. A study of nearly 300 design and engineering professionals found that 92% of respondents say they’re experiencing at least one form of increased complexity. Moreover, 76% say they’re […]
In this blog, we recap the “Implementing Requirements Management for ISO 21434” webinar. As the automotive industry becomes more complex and more connected, cybersecurity is emerging as a major concern, and therefore priority, for development teams. According to Juniper Research, there are 206 million cars on the road with embedded connectivity and by 2025, the […]
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 […]
If you’ve worked in product development for any time at all, you’ve probably heard the term “ISO” used in conjunction with the terms “standards” and “compliance” (along with a variety of four- and five-digit numbers). But what does that all mean, and how does it affect you? In this article, we will provide you with […]
Infographic: Jama Connect™ for Medical Device Development We’re excited to share our latest infographic for the Jama Connect for Medical Device Development solution which explains how Jama Connect can help accelerate innovation, maintain product quality, and manage the ever-changing complex regulations in medical device development. This is a single powerful platform for medical device teams […]