Jama Software

⏰ One week away! Join us on Tuesday, June 18 for an information-packed exploration of the notified body process and the implementation of the In Vitro Diagnostic Regulation (IVDR) technical documentation, hosted by Margot Borgel, Ph.D., Director, IVD Global Regulatory Affairs at RQM+ and Vincent Balgos, Director of Medical Device Solutions at Jama Software®. ✅ Ensure your technical documentation meets EU IVDR standards by registering HERE 👉https://ow.ly/L25V50SfFZ1 #IVDR #Compliance #NotifiedBodyExpectations

💡 Artificial intelligence (AI) is a topic that has infiltrated every aspect of society, causing a transformational shift (or the promise of one) in almost every landscape – and product development is no exception. AI has the potential to significantly improve productivity, innovation, and accuracy throughout the whole product development lifecycle, from ideation and defining requirements to commercialization. In this blog post, we’ll look at some of the different ways AI and ML will likely influence product development 👉 https://ow.ly/mccp50SfxWL #ai #productdevelopment #artificialintelligence

👋 How can you ensure your business and engineering are in sync? With LemonTree.Connect, users can synchronize requirements, model elements, and links and references between Application Lifecycle Management (ALM) and Model-Based System Engineering (MBSE) tools like Jama Connect® and Enterprise Architect (EA). 💡 Join us for our upcoming webinar “Bridging ALM and MBSE: Strategies for Seamless Integration,” on June 26 8:00 a.m. PT | 5:00 p.m. CEST, hosted by Philipp Kalenda, Head of Consulting & Training at LieberLieber and Cary Bryczek, Director of Solution Architecture at Jama Software® Attendees will gain a thorough understanding of these topics and more: ✅ How Jama Connect’s Live TraceabilityTM capabilities allows for seamless integration across best-of-breed tools. ✅ How leveraging Jama Connect Companion MBSE can act as a starting point for your MBSE efforts. ✅ How to create a workflow for deriving systems architecture based on requirements from Jama Connect. ✅ How LemonTree.Connect enables standard engineering domain practices for configuration management. ✅ How to facilitate streamlined evidence which proves your architecture is satisfying requirements. Don't miss this opportunity to discover how this powerful collaboration eliminates the gap between requirements engineering, system architecture, design, and product management! Register now to secure your spot! https://bit.ly/4aRm4V3

🚗 With the rise of connected vehicles and expanding attack surfaces, safeguarding against cybersecurity threats has never been more crucial. 🌟 In our new whitepaper, we explore how automotive and semiconductor teams can leverage requirements management tools to meet ISO/SAE 21434 standards while increasing visibility, collaboration, and review-cycle efficiency. Download the whitepaper now and gain insights into managing cybersecurity effectively in the automotive and semiconductor industries👉 https://ow.ly/8EzG50Sa35Y #cybersecurity #automotive #semiconductor

💡 Learn how you can supercharge your systems development process! In this Features in Five Integration Series video, Steven Pink – Senior Solutions Architect at Jama Software® – demonstrates integrating test results from TestRail with Jama Connect® ✅ Learn more 👉 https://ow.ly/vlIa50Sa3y0 #testrail #integration

🗣️ Prepare your technical documentation to meet EU IVDR standards! ✅ 👋 Due to the self-declaration process of previous directives, the implementation of the In Vitro Diagnostic Regulation (IVDR) in Europe presents a unique challenge for many IVD manufacturers. This is especially true for those attempting to enter the market for the first time or whose previous devices were self-declared. Many IVD manufacturers are unaware of the notified body expectations, particularly regarding the technical documentation requirements. 🗓️ Join us on Tuesday, June 18 for an information-packed exploration of the notified body process and IVDR technical documentation, hosted by Margot Borgel, Ph.D. Director, IVD Global Regulatory Affairs at RQM+ and Vincent Balgos, Director of Medical Device Solutions at Jama Software®. Ensure your technical documentation meets EU IVDR standards by registering HERE 👉 https://ow.ly/3PrH50Saaz5 #IVDR #Compliance #NotifiedBodyExpectations

🌟 Join us at the 34th Annual INCOSE International Symposium in Dublin from July 2-6, 2024! 🌟 💡While you're there, we encourage you to visit booth 32 and meet our experts Karl Mulcahy and Cary Bryczek. Take the opportunity to gain informative insights into Jama Connect's comprehensive approach to defining and managing Live Traceability™ throughout the entire lifecycle, and don't forget to collect some exclusive swag! 👋 Additionally, we invite you to attend our expert Cary Bryczek's live session, "Measuring Conformity to a Model-Based Systems Engineering Workflow" on Tuesday, July 2nd, from 11:30-11:50, where she'll discuss how achieving a model-centric view of your engineering data is the first step towards model-based systems engineering (MBSE). In this session, Cary will share how we help organizations understand data in their legacy tool (IBM® DOORS®) and then determine how to best transform the shape and size of that data into a model-based framework (Jama Connect®). For more details, visit https://ow.ly/8ZGy50S9Om6 - See you there! #INCOSE2024 #MBSE #JamaConnect #Engineering

👋 Interested in how smaller manufacturers are using technology to grow their businesses? 💡 In this curated blog, learn how cobots fit into reshoring and automation 👉 https://ow.ly/m6wQ50S8HVU #cobots #manufacturing

🔐 Tomorrow!!! Learn how to protect your data by joining us on Wednesday, June 5, for an informative webinar exploring the process of Model-Based Systems Engineering (MBSE) migration to minimize the risk of data loss. 🌟 👉 Register now and learn about the risks associated with legacy requirements management tools and explore effective solutions for migration > https://ow.ly/qCBq50S0TEU #MBSE #DataMigration

👋 We need your input! 💡 Jama Software is thrilled to host an upcoming interview with Bijan Elahi, a distinguished expert in medical device risk management. Join us as we delve into the critical topics of designing with cybersecurity and patient safety in mind. Bijan's extensive experience and insights will shed light on how to navigate the complex landscape of medical device development while ensuring the highest standards of safety and security. Prior to the interview, we’re asking our audience to weigh in on what they want to hear about the most 👇 👉 Significance of a comprehensive risk management approach, including safety + security, for medical devices 👉 Interfaces between safety and security risk management processes, and how they interact/complement each other. 👉 Upcoming industry trends that impact risk management (safety, security) like AI/ML, rise in connected devices, wearables devices. Or if you have specific questions you’d like us to ask Bijan during this session, drop them into the comments below!