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191Blog Post

Jama Connect® vs. IBM® DOORS®: Industry Templates: A User Experience Roundtable Chat

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Jama Connect® vs. IBM®DOORS®: Industry Templates: A User Experience Roundtable Chat Increasing industry challenges and complexities are pushing innovative organizations to consider modernizing the tool(s) they use for requirements management (RM). In this blog series, Jama Connect® vs. IBM® DOORS®: A User Experience Roundtable Chat, we’ll present several information-packed video blogs covering the challenges that […]

192Press Release

Jama Software® Is the First to Deliver a Complete Requirements Authoring Solution

Jama Software® Is the First to Deliver a Complete Requirements Authoring Solution Requirements can now be authored in free text form, natural language analyzed, and managed as distinct items Portland, Ore., USA, Jan 18, 2023 – Jama Software®, the industry-leading requirements management and traceability solution provider, announces enhancements to Jama Connect®’s user experience. As part […]

193Blog Post

Jama Software® Is the First to Deliver a Complete Requirements Authoring Solution

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Jama Software® Is the First to Deliver a Complete Requirements Authoring Solution Requirements can now be authored in free text form, natural language analyzed, and managed as distinct items Jama Software®, the industry-leading requirements management and traceability solution provider, has announced enhancements to Jama Connect®’s user experience. As part of the update, Jama Connect now […]

194Blog Post

Common Pitfalls in Change Control Traceability and How to Compensate

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Common Pitfalls in Change Control Traceability and How to Compensate Intro Change is constant, especially in the medical device lifecycle. These changes can be initiated by a manufacturer voluntarily, such as exchanging a component to decrease overall COGS or improve reliability. Or occur involuntarily, like when a supplier discontinues a component or regulations are revised. […]

195Blog Post

Understanding Integrated Risk Management for Medical Devices

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In this blog, we’ll recap our whitepaper, “Understanding Integrated Risk Management for Medical Devices” – To read the entire paper, click HERE. Understanding Integrated Risk Management for Medical Devices Knowledge on best practices, how to integrate risk-based thinking into product development cycles, and the importance of having end-to-end traceability to improve risk management, shared by […]

196Blog Post

Jama Connect® for Robotics: Accelerate Innovation and Simplify Functional Safety Compliance

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Jama Connect® for Robotics Jama Connect® for Robotics provides a single platform for development teams to manage requirements, test, and functional safety throughout the product development lifecycle in the robotics industry. The Jama Connect Robotics Solution is a complete set of frameworks, example projects, and procedural, export, and configuration documentation intended to accelerate the implementation […]

197Blog Post

[Webinar Recap] Write Better Requirements with Jama Connect Advisor™

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In this blog, we recap the “Write Better Requirements with Jama Connect Advisor™” webinar. Successful product delivery starts with having the right user needs and requirements. Efficient, precise, and professionally written requirements form the foundation of the product development process so that various teams (design, software, and hardware systems) can all work together with a […]

199Blog Post

Vave Health Decides to Migrate to Jama Connect® to Accelerate Development and FDA Clearance

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In this blog, we partially recap this customer story, “Vave Health Migrates to Jama Connect® to Accelerate Development and FDA Clearance” Read the entire story HERE. Vave Health is committed to revolutionizing the physician-patient experience through innovative, industry-transforming technologies. Their innovative handheld ultrasound device packs the ability to wirelessly connect with your Android or iOS […]

200Blog Post

CE Marking for Medical Device Software: A Step-By-Step Guide

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Jama Software is always looking for news that would benefit and inform our industry partners. As such, we’ve curated a series of customer and industry spotlight articles that we found insightful. In this blog post, we share an article, sourced from Spyrosoft, titled “CE marking for Medical Device Software: a step-by-step guide” – originally authored […]