We at Jama Software have been working with industry leading medical device companies over the past decade streamlining their device product development, simplifying regulatory submissions and audit preparations, and accelerating time to market.
Today we bring that partnership to the next level with a new solution designed to help engineering teams better manage device requirements, risk and design control all on one powerful platform. The newest release makes regulatory submissions and audit preparations a straightforward process, speeding time-to-market deployment with no reduction in quality.
With Jama for Medical Device Development, you can:
- Easily demonstrate traceability
- Manage risk analysis
- Maintain audit trails and export data
- Improve product development with reuse and baseline management
- Streamline compliant reviews and approvals
- Manage design verification and validation
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 ISO 13485:2016, 21 CFR 820.30, and ISO 14971:2019, while applying a proven Systems Engineering approach to product development. When you purchase Jama Connect for Medical Device Development, our consultants partner with you to adapt the solution to fit your product delivery process and build adoption of Jama Connect within your organization. Contact your Account Manager to learn more.
READ THE PRESS RELEASE [https://www.jamasoftware.com/company/press/jama-software-announces-jama-connect-for-medical-device-development/]
Visit https://www.jamasoftware.com/solutions/medical-device/ to learn more about Jama Software for Medical Device Development.