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41Blog Post

2023 Predictions for Medical Device Product Development

As we enter 2023, Jama Software asked selected thought leaders – both internal Jama Software employees and our external partners – across various industries for the trends and events they foresee unfolding over the next year and beyond. In the fourth part of our five-part series, we asked Shawnnah Monterrey, CEO at BeanStock Ventures – […]

42Blog Post

2023 Predictions for Industrial and Consumer Electronics Product Development

As we enter 2023, Jama Software® asked selected thought leaders – both internal Jama Software employees and our external partners – across various industries for the trends and events they foresee unfolding over the next year and beyond. In the third part of our five-part series, we asked Beau-Colby Thomson – Associate Account Executive at […]

43Blog Post

2023 Predictions for Aerospace & Defense Product Development

As we enter 2023, Jama Software® asked selected thought leaders – both internal Jama Software employees and our external partners – across various industries for the trends and events they foresee unfolding over the next year and beyond. In the second part of our five-part series, we asked Craig E. Miller, PhD – Principal Engineer […]

44Blog Post

When Evaluating Product Development Software Tools, Not All Cloud is Equal

In this blog, we’ll recap our whitepaper, “When Evaluating Product Development Software Tools, Not All Cloud is Equal” – To download the entire whitepaper, click HERE. When Evaluating Product Development Software Tools, Not All Cloud is Equal As product development has become increasingly complex to manage across siloed teams and tools, the need for organizations […]

45Blog Post

The New EU In Vitro Diagnostic Regulation: What’s Changing and What You Need to Know: Part 2

This is part 2 of a two-part blog series covering our whitepaper, “The New EU In Vitro Diagnostic Regulation: What’s Changing and What You Need to Know” written by Vincent Balgos, Medial Solution Manager at Jama Software. In this paper, Vincent discusses the In Vitro Diagnostic Regulation (IVDR), developed by the EU Commission (CE), which […]

46Blog Post

The New EU In Vitro Diagnostic Regulation: What’s Changing and What You Need to Know: Part 1

This is part 1 of a two-part blog series covering our whitepaper, “The New EU In Vitro Diagnostic Regulation: What’s Changing and What You Need to Know” written by Vincent Balgos, Medial Solution Manager at Jama Software. In this paper, Vincent discusses the In Vitro Diagnostic Regulation (IVDR), developed by the EU Commission (CE), which […]

47Blog Post

[Webinar Recap] Driving Business Outcomes with Jama Software’s Success Programs

In this blog, we recap the “Driving Business Outcomes with Jama Software’s Success Programs” webinar. When you buy Jama Connect, you’re not just buying the #1 requirements management solution on the market. Our Customer Success team stands behind you, delivering the expertise, guidance, and resources you need to see a quick return on your investment […]

48Blog Post

[Webinar Recap] Implementing Requirements Management for ISO 21434

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 […]

49Blog 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 […]