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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 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.
In this eBook, learn to reduce project risk in the development process by implementing Living Requirements™ management forming a digital thread through siloed development, test, and risk activities.
Learn how Jama Connect helps MPS efficiently manage complex requirements with greater visibility, more efficiencies, and structured collaboration across teams.
Accelerate digital engineering and enable collaboration for airborne systems development with Jama Connect for Airborne Systems – Getting Started Edition.
In this datasheet, we’ll demonstrate how to reduce the time required for validation for automotive teams with the Functional Safety Kit for Jama Connect.
Learn how the functional safety standard, ISO 26262, applies to automotive developers in this white paper that also looks at its recent updates, including ISO 26262 2018.
How can you better manage projects when scope changes? Learn best practices around collaboration, traceability, test coverage, and change management.
This paper looks at the challenges companies face when addressing the intersection of functional safety and efficient, collaborative product development.
Learn how using a single platform can help accelerate innovation, maintain consistency and high product quality, and manage ever-changing complex regulations in medical device development.
Tips for Medical Device Companies, Interested in Risk Techniques following ISO 14971, ISO 13485, FMEA, FTA, and 21 CFR Part 820.
Failure Modes and Effects Analysis (FMEA) is a common and trusted risk assessment tool used by systems and product development teams to manage risk early.
In this blog post, we explain how to improve design control and risk management in medical device development by moving away from a document-based system.
Last week, Jama Software launched Jama Connect for Medical Device Development, which helps teams speed time-to-market without compromising quality or compliance. In our experience working with...
Introducing Jama Connect for Airborne Systems, built to facilitate digital engineering and accelerates time-to-market in the development of aircraft systems
In this webinar you’ll learn how to move beyond the frustrations of document-based requirement systems to streamline your medical device development
Building and then bringing a medical device to market as quickly as possible—all while preserving acceptable levels of quality and regulatory compliance—requires adept medical device risk...