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Introducing Jama Connect for Automotive, our new solution designed specifically to accelerate product development for automotive engineering teams in the autonomous, electric, and traditional vehicle space.
In this post, we discuss how as product development processes become more complex, traditional document-based requirements management shows its limitations.
Based on our work with hundreds of medical device developers, we’ve compiled this guide to navigating the complexity of medical device compliance.
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.
In this blog, we answer the commonly asked question, “what is product development lifecycle management” and cover best practices for product developers.
While writing requirements is both an art and a science that will vary by context, here are five best practices for writing crystal clear requirements.
In this post, we’ll explore how Jama Connect for Medical Device Development is designed to help you get ramped up quickly with a platform, training, and documentation aligned to industry regulations while applying a proven systems engineering approach to product development.
As part of our ongoing series of Ask Jama webinars, covering customer questions and best practices, this webinar addresses release management options.
Medical device manufacturers have a lot to keep track of these days. Between ongoing device development and preparing for the impending EU MDR, it’s more important than ever to maximize every partnership.
Improve collaboration, quality, and delivery in medical device development by freeing your teams from document-based design control and risk management.