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®
ByAtef 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....
Read More
Jama Connect® Stands Alone as the Leader in Requirements Management Software
ByJama 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...
Read More
Jama Connect® Features in Five: Live Trace Explorer™
ByFrancis 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...
Read More
2025 Expert Predictions for Aerospace and Defense: AI, Sustainability, and the Next Frontier
ByJama 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...
Read More
Jama Connect® Features in Five: Jama Connect Interchange™ – What Sets Us Apart
ByMario 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...
Read More
Traceable Agile™ – Speed AND Quality Are Possible for Software Factories in Safety-critical Industries
ByMarc 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...
Read More
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 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