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This is a private community for users running the Medical Devices solution of Jama Connect®.
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Hi! I'm working on a velocity report that seems to run fine on smaller item sets but fails to complete on large sets of items (~2000 items). The report starts running but does not complete, just shows as "running" indefinitely. The report does involve pulling in related items, calculations on fields, etc. Not sure if that…
All the items under requirement have both unique string and integer ids, and they are only accessible by the integer ids from the URL like: "https://<sometext>.jamacloud.com/perspective.req#/items/10108". These integer ids are not exported in the reqif file and hence difficult to navigate from the Simulink requirement app.…
I would like to know if clicking the "Start Test Run" button in the Execute Test window will generate an event that could be captured by REST APIs? The intention is to build a setup where clicking "Start Test Run" triggers a suite of tests on a local system.
What methods does everyone use to tie two requirements together aside from using the Relate function? The following comes to mind, but just want to check with everyone else: Using Tags Having a field attribute to the requirement. This attribute would be a custom field that is Item of Type.
I am missing the "Test Management - Improved Test Cycle Management" (see release notes 9.17 cloud). Please add
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Jama Software is aware of Microsoft Exchange's upcoming retirement of using Basic authentication for SMTP affecting our self hosted customers. This will be handled similar to Microsoft Exchange's retirement of Basic authentication for IMAP in Dec of 2022. The update will be included in the upcoming spring release currently…
Jama Connect customers, please take notice that Jama Software has updated its Acceptable Use Policy, located at https://www.jamasoftware.com/legal. Compliance with the Acceptable Use Policy is required under your agreement with Jama Software. If you have any questions or concerns about this updated policy, please feel free…
Audience: Jama Software® customers who have purchased industry-specific frameworks, data exchange, Jama Connect Interchange™, Functional Safety Kit (FSK), and Jama Validation Kit (JVK). Products Applicable: Jama Connect®, Jama Connect Interchange™, Data Exchange Use Case Access to paid-for community content for Jama…
Systems Engineering MedTech Challenges Implementing systems engineering (SE) practices in MedTech presents unique challenges. From aligning with regulatory standards like ISO 13485 to managing time-to-market pressures and technical complexity, MedTech professionals must navigate a highly regulated and rapidly evolving environment. In this webinar, industry experts Mike Johnson, Trainer & Co-Founder of SE-Training GmbH and Vincent […]
The New ARP4754B and Techniques in Jama Connect® for Airborne Systems ARP4754B, released on December 20, 2023, is a standard from SAE International that provides recommendations for the development of civil aircraft and systems, focusing on ensuring safety and compliance with regulations. It covers the entire aircraft development cycle, from system requirements through verification and […]
Understanding ISO 13849: The Foundation of Functional Safety in the Machinery Sector Like many industries, functional safety is a critical part of machinery design – ensuring the protection of operators, equipment (and surrounding environments) from hazardous situations. To help maintain functional safety in industrial manufacturing, most organizations use ISO 13849, a globally recognized standard that […]
Jama Connect Features in Five: Release Management via Reuse & Synchronization Learn how you can supercharge your systems development process! In this blog series, we’re pulling back the curtains to give you a look at a few of Jama Connect’s powerful features… in under five minutes. In this Features in Five video, Máté Hársing, Solutions […]
9 Strategies To Overcome Challenges In The EU Medical Device Market In 2025 And Beyond Global frameworks offer valuable insights for Europe as the region is currently working to refine its regulatory systems. While Europe is a significant player in the medical device market, the MDR transition has created challenges driven in part by higher […]
