Compliance & Regulation
On April 27, 2023
- Reading Time 5 min
What is a Trial Master File in the Medical Device Industry?
Traceable MBSE™ in Action: Integrating Sparx Enterprise Architect with Jama Connect®
By Atef Ghribi
/ February 20, 2025
Traceable MBSE™ in Action: Integrating Sparx Enterprise Architect with Jama Connect® In the complex systems engineering landscape, maintaining Model-Based Systems Engineering (MBSE) across requirements and architecture is a major challenge....
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Jama Connect® Stands Alone as the Leader in Requirements Management Software
By Jama Software
/ January 21, 2025
Jama Connect® Stands Alone as the Leader in Requirements Management Software We are thrilled to share that Jama Connect has been named the Overall Leader in G2®’s Winter 2025 Grid...
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Jama Connect® Features in Five: Live Trace Explorer™
By Francis Trudeau
/ January 3, 2025
Jama Connect Features in Five: Live Trace Explorer Learn how you can supercharge your systems development process! In this blog series, we’re pulling back the curtains to give you a...
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2025 Expert Predictions for Aerospace and Defense: AI, Sustainability, and the Next Frontier
By Jama Software
/ January 2, 2025
2025 Expert Predictions for Aerospace and Defense: AI, Sustainability, and the Next Frontier Aerospace and defense are at the cusp of revolutionary changes, driven by advancements in artificial intelligence, autonomous...
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Jama Connect® Features in Five: Jama Connect Interchange™ – What Sets Us Apart
By Mario Maldari
/ September 6, 2024
Jama Connect Features in Five: Jama Connect Interchange - What Sets Us Apart Learn how you can supercharge your systems development process! In this blog series, we’re pulling back the...
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Traceable Agile™ – Speed AND Quality Are Possible for Software Factories in Safety-critical Industries
By Marc Osofsky
/ October 3, 2023
Traceable Agile – Speed AND Quality Are Possible for Software Factories in Safety-critical Industries Automotive, aerospace and defense, and industrial companies have largely adopted Agile within rapidly growing software...
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Product Development & Management
On April 26, 2023
- Reading Time 3 min
FDA Moving Ahead with Rulemaking On Lab Developed Tests Without Waiting for Congress: BioWorld
Compliance & Regulation
On April 25, 2023
- Reading Time 5 min
Introduction to ISO 24089: Your Ultimate Guide to Understanding and Implementing This New Standard for Automotive
![[Webinar Recap] An Overview of the EU Medical Device Regulation (MDR) and In-Vitro Device Regulation (IVDR)](https://www.jamasoftware.com/media/2023/04/BLOG-RECAP-Medical-Device-Webinar-Social-Image.png "[Webinar Recap] An Overview of the EU Medical Device Regulation (MDR) and In-Vitro Device Regulation (IVDR)")
Risk Management
On April 20, 2023
- Reading Time 8 min
[Webinar Recap] An Overview of the EU Medical Device Regulation (MDR) and In-Vitro Device Regulation (IVDR)
Compliance & Regulation
On April 18, 2023
- Reading Time 5 min
Streamlining Defense Contract Bid Document Deliverables with Jama Connect®
Jama Software Company and Community News
On April 14, 2023
- Reading Time 6 min
Jama Connect® Features in Five: Using Jama Connect with a Quality Management System (QMS) for Medical Device & Life Sciences
Product Development & Management
On April 13, 2023
- Reading Time 3 min
FDA Class I Recalls Hit 15-year High in 2022
Compliance & Regulation
On April 11, 2023
- Reading Time 7 min
The Top Challenges in Industrial Manufacturing and Consumer Electronic Development
Product Development & Management
On April 4, 2023
- Reading Time 8 min
Digital Transformation of Verification Process for Faster Aircraft Certification
![[Webinar Recap] Why it Makes Sense to Store Cybersecurity Risk Management Items Inside a Requirements Management System](https://www.jamasoftware.com/media/2023/03/Cybersecurity-Risk-RM-.png "[Webinar Recap] Why it Makes Sense to Store Cybersecurity Risk Management Items Inside a Requirements Management System")
Risk Management
On March 30, 2023
- Reading Time 8 min
[Webinar Recap] Why it Makes Sense to Store Cybersecurity Risk Management Items Inside a Requirements Management System
Other
On March 28, 2023
- Reading Time 5 min
Practical Guide for Implementing Software Validation in Medical Devices: From FDA Guidance to Real-World Application – Part 2
Product Development & Management
On March 23, 2023
- Reading Time 4 min
Medtech Industry Relieved as Europe’s MDR Extension Nears Final Approval