magniX, Selects Jama Connect® for Its Ease of Use and Quick Deployment

Read this comprehensive guide to understanding ANSI/AAMI SW96:2023 and mitigating security risks in medical device development.

In this eBook, we look at the importance of avionics cybersecurity and demonstrate how DO-326A provides compliance guidelines to address the vulnerabilities of avionics systems.

In this solution overview, learn how to streamline compliance and collaboration with the Jama Connect® Library for DoD Range Safety Requirements.

In this datasheet, we cover the benefits of a Jama Connect cloud deployment, and the features that set it apart from similar tools in its category.

Selecting an engineering tool provider is a big decision. In this datasheet, we cover four key considerations that organizations must think about prior to selecting a cloud-based engineering tool.

In this guide, we take a comprehensive look at ISO/IEC/IEEE 15288:2015 goals, standards, and tools that help achieve compliance.

In this datasheet, we cover how teams can accelerate innovation and simplify functional safety compliance in robotics development by leveraging Jama Connect® for Robotics.

See why Vave Health chose Jama Connect® to automate and streamline processes in order to maintain efficient release cadences, manage change, and ensure full verification and validation (V&V) coverage.

In this customer story, we cover how Microsure leverages Jama Connect® to involve all team members in development, efficiently manage change, and quickly provide necessary regulatory documentation.

Learn how to address cybersecurity risks in the design & development of car electronics with ISO SAE 21434 and how Jama Software® can help you meet this important standard for automotive development.

In this eBook, we provide an overview of the Research Use Only (RUO) label, how it differs from similar, adjacent labels, its appropriate use, and the consequences of mislabeling products RUO.

In this customer story, we look at why Convergent Dental chose Jama Connect to manage compliance through in-depth reviews and to save valuable engineering time

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).

REGENT Craft leverages Jama Connect for requirements management in order to adhere to rigorous safety standards, speed through design reviews, and get to market faster.