Whitepapers

Download this report to learn more about why, among other awards, Jama Connect® was selected as the overall leader in the Summer 2022 G2® Grid® Report for requirements management software.

Learn about the new draft guidance for Premarket Submissions for Device Software Functions, the documentation levels, and the software documentation elements required for medical device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.

Jama Connect® was again named the overall leader in the Spring 2022 G2 Grid® Report for Requirements Management Software! Learn why in this free downloadable report.

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.

In this whitepaper, we examine why organizations move away from legacy requirements management tools, the benefits of making the switch, and how to successfully migrate.

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.

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 whitepaper, written in conjunction with the avionics experts at AFuzion, we examine this important safety standard and the key components of ARP4761A.

In this quickstart guide, we describe the building blocks within the Companion MBSE framework and show you how to put the solution together in your own Jama Connect server.

G2 named Jama Connect® the leader in requirements management software in the Winter 2022 Grid® Report. Download the full report to see why we received this honor and several additional badges!

Read this whitepaper to learn more about the impact of poor requirement definition and traceability on time, scope, and budget – and how reducing requirement debt reduces project risk.

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.

In this paper, we examine how and why the Easy Approach to Requirements Engineering Syntax (EARS) notation enables cross-team collaboration, improves product requirements, and reduces project risk.

In this whitepaper, experts from Beanstock Ventures cover the emergence of Software as a Medical Device (SaMD), potential challenges for digital health technology, and recommendations to address them.

Today’s products are becoming increasingly complex and software-intensive – this is one of the main reasons that MBSE has emerged as the standard approach to digital transformation.

The new Medical Device Regulation (EU MDR) addresses software as a medical device (SaMD), as well as other products. Here, we cover the new regulations and highlight the most important changes.

In this paper, we examine the role legacy requirements management solutions play in introducing project risk to the product development process, and look at modern alternatives to IBM DOORS.