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 introduce our 6-part deminar series where we’ll cover key features and capabilities of Jama Connect, seamless integrations, best practices, and more.
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.
Impact analysis is a key aspect of responsible requirements management. It provides an accurate understanding of the implications of a proposed change, which helps the teams make informed business decisions about which proposals to approve. The analysis examines the proposed change to identify components that might have to be created, modified, or discarded and to […]
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.