Consistent product quality and safety proves to be the top challenge for innovators throughout the medical device development lifecycle. Constantly evolving regulations and the new complexities presented by connected devices makes management of these shifting complexities difficult. In this eBook, we share what to look for in a platform and share how Jama Connect for Medical Device Development can help teams align to industry regulations quickly, simplify regulatory submissions and audit preparations, and accelerate time to market. You will also learn:
The context around common product development pain points
To uncover the savings from a modern requirements management and traceability solution and calculate the ROI
Five key elements to evaluate requirements management platforms
How to narrow down your options with an essential-feature comparison checklist
Best Practices Guide for Writing Requirements
In this eBook, our experts explain how to write clear, concise requirements that drive greater transparency...
Optimize Engineering Team Collaboration to Streamline Product Development
Learn how optimizing your engineering team’s collaboration can streamline the product development process, ...