Author Bio
Cybersecurity in the Air: Addressing Modern Threats with DO-326A Introduction Not long ago, getting on an airplane meant being largely out of touch with everyone on the ground for the duration of one’s flight. Of course, there were in-flight telephones for those who could afford them, and pilots could connect with personnel on the ground […]
Why Relying Solely on Documents Won’t Cut It in the World of Complex Product, Systems, and Software Unless your organization’s business model is built on a foundation of inefficiency, you should not be using disparate documents for managing requirements. Whether it’s Microsoft Word, Excel, or a combination of both, trying to wrangle your product’s requirements […]
Global Industry Leading Automotive Application Developer dSPACE Migrates from Legacy Requirements Management Platform to Jama Connect® As part of a global modernization initiative, dSPACE partners with Jama Software® to migrate decades of data, increase collaboration, simplify compliance, and integrate processes across best-of-breed tools. About dSPACE Founded: 1988 in Paderborn, Germany (North Rhine-Westphalia) Expertise: Solutions for […]
Leading Quantum Computing Company, IonQ, Selects Jama Connect® to Decrease Review Cycles, Reduce Rework, and Improve Communication and Collaboration With a return on their investment in less than six months, the IonQ team is confident they made the right selection. About IonQ: Founded in 2015 by Chris Monroe and Jungsang Kim to “build the world’s […]
Using Jama to manage requirements and Jira to monitor tasks separately is a totally viable solution for many product companies. Those forward-thinking businesses who take advantage of the powerful integration between the two see much stronger management of complexity, traceability, requirements and progress tracking.
UK regulators name 3 approved bodies to ease device certification bottleneck A MHRA leader hailed the action as “almost doubling capacity for medical device assessment in the U.K.” Dive Brief: The Medicines and Healthcare Products Regulatory Agency (MHRA) has designated three more bodies to certify medical devices in the U.K. As a result of Brexit, […]
Unlocking the Potential: The Importance of Software Defined Vehicles Explained Introduction The automotive industry is undergoing a massive transformation, driven by technology. One of the most exciting developments is the concept of Software Defined Vehicles (SDVs). In this blog post, we will explore the importance of SDVs and how they are revolutionizing the automotive landscape. […]
Best Practices for Verification and Validation in Product Development In the competitive landscape of modern product development, ensuring the reliability and quality of the product is essential to meet customer – and stakeholder – expectations and regulatory requirements. Verification and validation (V&V) are two crucial processes that play a pivotal role in achieving these goals. […]
Q&A: How Monogram’s CEO plans to disrupt robotic joint replacement surgery The robot developer’s CEO, Benjamin Sexson, tells MedTech Dive why he believes the orthopedics market needs a fresh approach to joint reconstruction. Seven-year-old surgical robotics company Monogram Orthopedics, which went public in May, is aiming to take on medtech heavyweights such as Stryker and […]
Embracing the Future of Healthcare: Exploring the Internet of Medical Things (IoMT) Internet connected devices, part of the Internet of Things (IoT) are everywhere. These devices, often referred to as “smart” devices are in our homes, cars, offices, and gyms. Therefore, it is no surprise that smart devices are making their way into our healthcare […]