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One of the biggest challenges of developing new automotive products is meeting functional safety standards like ISO 26262.
Watch industry safety certification experts TÜV SÜD, and Jama Software discuss:
4:28Part one of this two-part video series demonstrates the latest solution offerings for Medical Device & Life Sciences in Jama Connect.
57:05In this webinar, learn more about Threat and Risk Analysis (TARA), its importance in achieving ISO 21434 compliance, and how a requirements management solution can help.
Learn more about simplifying complex financial development, deployments, and migrations with Jama Connect® by enabling process efficiency and real-time collaboration to accelerate time to market.
In this Traceability Score™ research project, we explore the impact of late requirements on projects, and how maintaining a high Traceability Score dramatically reduces the risk of late requirements.
7:59In this Features in Five video, we do go beyond the promised five-minute format to include an information-packed session on how risk management integrates with Jama Connect for Medical Device.
43:42In this webinar, we’ll demonstrate how Jama Connect® creates Live Traceability™ through siloed development, test, and risk activities to effectively reduce risk in the product development process.
In this paper, industry experts share best practices for integrated risk management, how to integrate risk-based thinking into product development cycles, and the importance of traceability.
1:02:57In this webinar, experts will walk through how to take a comprehensive and integrated approach to risk management for medical device development – and the benefits.
In this medical device research study from Axendia, a leading Life-Sciences Analyst firm, see how ineffective requirements management can negatively impact budgets, traceability, and V&V activities.
This is Part 2 of a series examining the role legacy requirements management solutions, such as IBM® DOORS®, play in introducing project risk to the product development process. To read Part 1, ...
In this whitepaper, experts from Beanstock Ventures cover the emergence of Software as a Medical Device (SaMD), potential challenges for digital health technology, and recommendations to address them.
Congratulations! Your organization has gained regulatory approval and launched its medical device product. The ‘History’ in Design History File may elicit impressions that all those design and...
As a medical device product development consultant, I often see start-up companies having trouble deciding what to prioritize – design controls and risk management or the quality management system...
In this post, we look at how Teledyne e2v leverages Jama Connect for improved communication and better risk management. Teledyne e2v is a global leader in specialized components and subsystems...
In this paper, we examine the role legacy requirements management solutions play in introducing project risk to the product development process, and look at modern alternatives to IBM DOORS.
Design Controls have been an FDA Quality System Regulation since 1997. Having worked on developing products in the regulated medical device industry for over 35 years, I have compiled a list of...
In this customer story, we look at why magniX chose Jama Connect to help modernize their requirements management program and demonstrate compliance with standards.
Machine Learning in Software as a Medical Device Machine learning (ML), a subset of artificial intelligence, has become integral across software in all industries, and the medical and life science...
Download this eBook to see how software teams are using Jama Connect’s single requirements and traceability platform to accelerate time to market.
Download this datasheet to see how software development teams are using Jama Connect’s single requirements platform to accelerate time to market.
