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Modern requirements management can help you respond quickly to new regulations, reduce uncertainty, and bring more cost-effective digital health solutions to market faster.
See how Jama Connect™ for Digital Health helps medical device development teams reduce the effort required to achieve regulatory compliance throughout the development process.
2:53Jama Connect® for Financial Services and Insurance teams empowers your software teams with a platform that helps lower development costs, reduce cycle times, and minimize regulatory disruption.
What is ASPICE? Download our Automotive SPICE guide for a comprehensive look at ASPICE goals, requirements, and achieving compliance in automotive development.
Download this eBook to learn how medical device developers can prepare and implement the necessary changes to achieve compliance with the new EU MDR regulations.
In this customer story, we walk through why Telesat selected Jama Connect as part of an overall investment in engineering processes and tools for its satellite constellation project.
See how the Jama Connect® FMEA Framework assists automotive development teams when conducting comprehensive Failure Mode and Effects Analysis in this comprehensive datasheet.
In this eBook, we’ll address how implementing Living Requirements™ management forms a digital thread through siloed development, test, and risk activities.
45:08In this webinar, we’ll cover the Jama Connect for Airborne Systems solution and how it enables safety-critical engineering for aerospace and defense aircraft development.
Enable cross-discipline collaboration and an integrated digital approach to accelerate systems development with Jama Connect for Air, Land, Sea, and Space Systems.
In this customer story, we look at how Jama Software helps ETAS NI Systems, innovator in the automotive sector, customize Jama Connect for their specific needs and get up and running quickly.
1:48In this video, we demonstrate how Living Requirements Management in Jama Connect enables cross-team collaboration and reduces the risk of negative product outcomes.
In this whitepaper, written in conjunction with the avionics experts at AFuzion, we examine this important safety standard and the key components of ARP4761A.
Download this datasheet to learn how to analyze and mitigate potential failure modes or risks for medical device development to ensure quality and accelerate time to market.
For this information-packed eBook, Jama Software teamed up with Beanstock Ventures to weigh in on trends and predictions for medical device development in the new year and beyond.
Learn more about how the Finnish Red Cross Blood Service leverages Jama Connect to modernize their processes, improve communication, and shorten review cycles.
Read this customer story to see how Jama Software helps automotive innovator Arteris IP simplify complex semiconductor IP development.
Read this guide to learn the purpose of ISO 13485 and requirements for adherence, the difference between ISO 13485 and other medical device standards, and get key steps to adoption and certification.
Check out this handy checklist to make sure you're getting everything you need in a requirements management solution.
1:03:39In this webinar, we’ll review the details of the latest product roadmap enhancements related to baselines and how to get the most out of Jama Connect’s baseline capabilities.