OBEO PUBLICATION FOR CAPELLA + JAMA CONNECT GIVES YOU MORE INCREASE DEVELOPMENT EFFICIENCY: Replace error-prone manual checking of new and changed items with automated updates across the development toolchain and throughout the development lifecycle. SIMPLIFY VISIBILITY, COLLABORATION, AND REVIEWS: Make it easier for stakeholders to view and interact with requirements and test management data in […]
Standardizing Requirements Management Across the Organization Learn how to prevent costly production failures with standardized requirements management. A survey by Engineering.com revealed that a staggering 83% of companies faced production outcome failures — such as significant delays, cost overruns, product defects, compliance gaps, recalls, omitted requirements, and extensive rework — often stemming from inadequate requirements […]
Streamline Complex Product Quality, Compliance, and Time-to-completion with Jama Connect for Semiconductors Semiconductor companies face increasing challenges in developing their next-generation products and product families. Product customization and resulting variants make it difficult for development teams to establish and maintain traceability throughout their engineering workflows, especially when design changes occur frequently. This often results in […]
What Is IBM DOORS Software? Features, Limitations, and Why Teams Are Switching If you’ve worked in aerospace, defense, or medical devices, you’ve almost certainly run into IBM DOORS. It’s long been one of the most widely used requirements management tools in regulated industries. But the engineering world has changed since DOORS was built, so a […]
When Change Impact Becomes Chaos: A Business Analyst’s Survival Guide Requirements change. It’s not a possibility. It’s a certainty. Priorities shift mid-sprint, regulators update compliance standards, and stakeholders introduce new dependencies long after a project has gained momentum. For business analysts (BAs), this constant flux creates a ripple effect that’s difficult to track and even […]
Transmutex Wastes No Time Choosing Jama Connect for Developing Nuclear Waste Recycling Systems “Jama Connect’s ease of use is a big plus for us because we have a lot of people inexperienced with requirements who can now author and review requirements without training or other meetings,” – ALEXANDRE CARVALHO, SYSTEMS ENGINEER, TRANSMUTEX ABOUT TRANSMUTEX Transmutex […]
IEC 62304 Edition 2: What to Expect and Why It Matters IEC 62304, the international standard governing medical device software lifecycle processes, is undergoing its first major revision in nearly 20 years. While the upcoming second edition aims to clarify requirements and better reflect modern software practices, it also intentionally preserves the stability manufacturers rely […]
The Simplification of the EU MDR: What MedTech Needs to Know The European Medical Device Regulation (EU MDR) continues to present challenges for quality and regulatory teams, as well as for the medical device industry more broadly, years after its publication. The updated legislation was introduced with the objective to improve patient safety and harmonize […]
SPAN Electrifies Its Product Development and Safety with Jama Connect “By implementing Jama Connect, our teams are able to maintain transparency across stakeholders, streamline communication, and ensure alignment on project goals. This integrated approach reduces redundant efforts and helps accelerate product development cycles while maintaining compliance and quality standards,” – Arnaldo Arancibia, Senior Staff Systems […]
Augmented intelligence in medicine Artificial intelligence vs. augmented intelligence The AMA House of Delegates uses the term augmented intelligence (AI) as a conceptualization of artificial intelligence that focuses on AI’s assistive role, emphasizing that its design enhances human intelligence rather than replaces it. AMA policy on AI development, deployment and use The AMA is committed […]
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