The “smarter” and more complex modern systems get, the more complicated the process required to build them becomes. Systems engineering teams working in regulated industries, such as semiconductors, aerospace, defense and medical device manufacturing—as well as highly disruptive industries focused on embedded systems—suffer an unfair share of the pain of product and systems development and management. In such industries, the margins of operation have always been tight, with little to no room for error, and maintaining product integrity is difficult.
Most Recent Flipbooks
In this Requirements Traceability Benchmark, we examine how traceability is measured, the benefits of Live Traceability™, and the best practices that separate top quartile performers from the rest.
Learn how the functional safety standard, ISO 26262, applies to automotive developers in this white paper that also looks at its recent updates, including ISO 26262 2018.
In this paper, we discuss how to leverage Jama Connect for MBSE to enable cross-discipline collaboration and a data-centric digital approach to prioritize the speed of delivery.
In this paper, we explore the advantages of cloud vs. on-premises software deployment and cover key considerations when choosing a cloud-based engineering tool.
In the Summer 2023 G2 Grid® Report for Requirements Management Software, Jama Connect® once again stood out as the clear leader. To learn why, get the complete report!
Document-centric processes have inconsistent data structures in unconnected tools. Learn how the Easy Approach to Requirements Syntax Notation can help support effective requirements management.
In this whitepaper, we cover the three main types of cloud for product development software, public, private, and hybrid, and discuss the advantages and disadvantages of each cloud deployment option.
In this whitepaper, our expert discusses key factors associated with successfully adopting MBSE and defines a roadmap tailored to your organization resulting in the successful adoption of MBSE.
This report on requirements management software compares Jama Connect vs DOORS Next. It is from SoftwareReviews (a division of Info-Tech Research Group) and is from the June 2022 Data Quadrant Award.
This report on requirements management software compares Jama Connect vs Polarion. It is from SoftwareReviews (a division of Info-Tech Research Group) and is from the June 2022 Data Quadrant Award.
This report on requirements management software compares Jama Connect vs codebeamer. It is from SoftwareReviews (a division of Info-Tech Research Group) and is from the June 2022 Data Quadrant Award.
In this whitepaper, written in conjunction with the avionics experts at AFuzion, we examine this important safety standard and the key components of ARP4761A.
In this medical device research study from Axendia, a leading Life-Sciences Analyst firm, see how ineffective requirements management can negatively impact budgets, traceability, and V&V activities.
In this whitepaper, we cover the goals, practices, and artifacts of each Capability Maturity Model Integration (CMMI) level and discuss how Live Traceability™ can help you progress up the 5 levels.
In this whitepaper, we explore some of the biggest challenges in the Architecture, Engineering, Construction, and Operations (AECO) industry and how Jama Connect® can help solve them.
Jama Connect® was again named far above all others as the standout leader in the Spring 2023 G2 Grid® Report for Requirements Management Software! Download the full report to see why!
From supply chain disruptions to digitization, read this whitepaper to learn more about what industrial manufacturing teams are up against and get expert suggestions for how to overcome them.
Learn about the new draft guidance for Premarket Submissions for Device Software Functions, the documentation levels, and the software documentation elements required for medical device development.
In this whitepaper, we’ll discuss how emerging In-Vitro Diagnostics (IVDs) will be developed, managed, and regulated in the EU and beyond according to the new In Vitro Diagnostic Regulation (IVDR).
In this comprehensive guide to the VALID Act, we examine the provisions and implications of the VALID Act and how it applies to product development and risk management for medical devices.