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91Blog Post

[Webinar Recap] Bridging the Gap in Insurance Product Development

Looking to bridge the gap in your insurance product development? Learn how carriers can utilize Jama Connect® to increase efficiency across the development process and more effectively deliver high quality products on time and on budget. During this informative session, Lianne Warford, Senior Business Analyst at LHW Consulting, and Steven Meadows, Principal Solutions Lead at […]

93Blog Post

Jama Software® Announces Largest Scale Achieved by Any Requirements Management Software

Jama Software® Announces Largest Scale Achieved by Any Requirements Management Software Jama Connect® 9.5 proven to scale to at least 10 million requirements in a single project to handle the largest product, systems, and software development efforts. Jama Software®, the industry-leading requirements management and traceability solution provider, has announced that Jama Connect® has set yet […]

94Press Release

Jama Software® Announces Largest Scale Achieved by Any Requirements Management Software

Jama Connect® 9.5 proven to scale to at least 10 million requirements in a single project to handle the largest product, systems, and software development efforts. PORTLAND, Ore – October 5, 2023 – Jama Software®, the industry-leading requirements management and traceability solution provider, announced today that Jama Connect® has set yet another scalability record with […]

95Blog Post

[Webinar Recap] Compliance Made Easy with Jama Connect® for Automotive and Semiconductor Development

Evaluate Your Compliance Against ASPICE, ISO 26262, or ISO 21434 with Diagnostic Services Offerings from Jama Software® During the webinar, experts Steve Rush, Principal Consultant, and Sampath Yerramalla, Senior Consultant, explored various service offerings within Jama Connect that provide insights into compliance status against these critical automotive standards. Key takeaways from this webinar: Learn about available […]

96Blog Post

Traceable Agile™ – Speed AND Quality Are Possible for Software Factories in Safety-critical Industries

  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 factories to speed time to market in order to stay competitive. These software factories have largely succeeded in speeding up software development for companies within […]

97Blog Post

UK Regulators Name 3 Approved Bodies to Ease Device Certification Bottleneck

UK regulators name 3 approved bodies to ease device certification bottleneck A MHRA leader hailed the action as “almost doubling capacity for medical device assessment in the U.K.” Dive Brief: The Medicines and Healthcare Products Regulatory Agency (MHRA) has designated three more bodies to certify medical devices in the U.K. As a result of Brexit, […]

98Blog Post

A New Partnership for Digital Design & Product Development eXcellence

Engineering Industries eXcellence Partners with Jama Software® to Drive Innovation in Digital Design and Product Development Across Industries PORTLAND, Ore. and CHICAGO, September 21, 2023 – Jama Software®, the industry-leading requirements management and traceability solution provider, and Engineering Group’s Industries eXcellence division, a global leader in the field of engineering services, design automation solutions, and […]

99Press Release

A New Partnership for Digital Design & Product Development eXcellence

Engineering Industries eXcellence Partners with Jama Software® to Drive Innovation in Digital Design and Product Development Across Industries PORTLAND, Ore. and CHICAGO, September 21, 2023 – Jama Software®, the industry-leading requirements management and traceability solution provider, and Engineering Group’s Industries eXcellence division, a global leader in the field of engineering services, design automation solutions, and […]

100Blog Post

EU Medical Device Regulation (EU MDR) FAQs: Industry Expert Insights

EU Medical Device Regulation (EU MDR) FAQs: Industry Expert Insights Are you grappling with the intricacies of the EU Medical Device Regulation (EU MDR) and searching for clear answers to your most pressing questions? Look no further! In this blog post, we’ve teamed up with subject matter expert Saby Ágai, Senior Professional Services Consultant at […]