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.
48:16In this webinar, learn how LDRA and Jama Software have teamed to apply a cybersecure-by-design approach to meeting DO-326A/DO-356A.
In this solution overview, learn how to streamline compliance and collaboration with the Jama Connect® Library for DoD Range Safety Requirements.
![[Webinar Recap] An Overview of the EU Medical Device Regulation (MDR) and In-Vitro Device Regulation (IVDR)](https://content.cdntwrk.com/mediaproxy?url=https%3A%2F%2Fwww.jamasoftware.com%2Fmedia%2F2023%2F04%2FBLOG-RECAP-Medical-Device-Webinar-Social-Image.png&size=1&version=1682006802&sig=1361cc9d7874231c89ed372d630e7528&default=hubs%2Ftilebg-blogs.jpg)
Looking to stay ahead of ever-evolving regulations governing medical devices? In this webinar, we discuss the continual rollout of the EU Medical Device Regulation (MDR) and In-Vitro Device...
46:50In this webinar, learn about observations and future considerations for medical device manufacturers in the EU market.
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).
Use this handy ROI calculator to learn how much inefficient review processes are costing you and how much budget can be reclaimed with a modern requirements management solution like Jama Connect.
Reclaim productive work time spent on manual activities, siloed data, sleuthing out change impact, etc. by implementing a modern requirements management solution into your development process.
Reduce risk across the development process and reclaim significant budget. Take a look at this ROI calculator to see how much you can save by reducing requirements-related defects by up to 40%!
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.
![[Webinar Recap] Understanding Integrated Risk Management For Medical Device](https://content.cdntwrk.com/mediaproxy?url=https%3A%2F%2Fwww.jamasoftware.com%2Fmedia%2F2022%2F07%2F2022-07-12_Understanding-Risk-Medical-Webinar-Social-Image.png&size=1&version=1674860437&sig=9b4d72067e480829dc43c8e6189b2bf6&default=hubs%2Ftilebg-blogs.jpg)
In this blog, we recap the “Understanding Integrated Risk Management for Medical Device” webinar. Companies involved in developing medical devices understand the importance of risk management, but...
