Medical device development is only growing more complex. Teams need end-to-end traceability, impact and risk analysis, intuitive reviews, and design verification and validation to support their entire product development process.
With Jama Connect™, Risk Management Center, and Medical Device Services, cross-functional medical device teams can innovate more efficiently while ensuring compliance with FDA and ISO regulations. This paper outlines how Jama Software can help you improve your product development process. You’ll learn how to:
- Navigate the complexity of medical device development
- Identify and mitigate risk throughout the development cycle
- Streamline collaboration and workflow
- Automate your documentation process for regulatory compliance