Whitepapers

Learn more about Breakthrough Insights, Best Practices, Industry Trends, Requirements Management, and more, through these in-depth reports.

  • The New EU In Vitro Diagnostic Regulation: What's Changing and What You Need to Know

    The New EU In Vitro Diagnostic Regulation: What's Changing and What You Need to Know

    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).

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  • G2 Grid Report for Requirements Management Software- Summer 2022

    G2 Grid Report for Requirements Management Software- Summer 2022

    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.

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  • FDA New Draft Guidance of Premarket Submissions for Medical Devices: Are you ready?

    FDA New Draft Guidance of Premarket Submissions for Medical Devices: Are you ready?

    Learn about the new draft guidance for Premarket Submissions for Device Software Functions, the documentation levels, and the software documentation elements required for medical device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

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  • G2 Grid Report for Requirements Management Software - Spring 2022

    G2 Grid Report for Requirements Management Software - Spring 2022

    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.

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  • Requirements Traceability Benchmark

    Requirements Traceability Benchmark

    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.

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  • The Limitations, Drawbacks, and Risks of Using Legacy Requirements Management Tools

    The Limitations, Drawbacks, and Risks of Using Legacy Requirements Management Tools

    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.

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  • Axendia Report: The Costly Impact of Ineffective Requirements Management

    Axendia Report: The Costly Impact of Ineffective Requirements Management

    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.

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  • FREE GUIDE: How to Get the Most From a Requirements Management Platform

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  • Testing the Requirements

    Testing the Requirements

    You can’t always visualize how a system will run just by reading requirements. That’s why early testing of requirements is such a powerful technique for catching ambiguities and errors.

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  • The Impact of ISO 26262 on Automotive Development

    The Impact of ISO 26262 on Automotive Development

    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.

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  • Integrating Jama Connect with Jira

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  • A Path to Model-Based Systems Engineering (MBSE) with Jama Connect

    A Path to Model-Based Systems Engineering (MBSE) with Jama Connect

    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.

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  • ARP4761A Introduction for Engineers and Managers

    ARP4761A Introduction for Engineers and Managers

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

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  • Jama Connect® Companion MBSE Quickstart Guide

    Jama Connect® Companion MBSE Quickstart Guide

    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.

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  • G2 Grid Report for Requirements Management Software- Winter 2022

    G2 Grid Report for Requirements Management Software- Winter 2022

    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!

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  • Tips to Manage Product Development Complexity and Traceability

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  • Requirements Debt: A Medical Product Program Risk

    Requirements Debt: A Medical Product Program Risk

    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.

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  • The Comprehensive Guide to Successfully Adopting Model-Based Systems Engineering (MBSE)

    The Comprehensive Guide to Successfully Adopting Model-Based Systems Engineering (MBSE)

    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.

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  • Adopting the EARS Notation to Improve Requirements Engineering

    Adopting the EARS Notation to Improve Requirements Engineering

    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.

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  • The Rapid Rise of Digital Health Technology: Challenges and Keys to Success

    The Rapid Rise of Digital Health Technology: Challenges and Keys to Success

    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.

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  • The Real Intent of Model-Based Systems Engineering (MBSE)- Keeping Up with Complexity

    The Real Intent of Model-Based Systems Engineering (MBSE)- Keeping Up with Complexity

    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.

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  • What the New Medical Device Regulations (EU MDR) Mean for You

    What the New Medical Device Regulations (EU MDR) Mean for You

    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.

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  • Why Move Away from IBM® DOORS® Legacy, and Why Now?

    Why Move Away from IBM® DOORS® Legacy, and Why Now?

    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.

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