Get to market sooner, stronger, and better prepared for future Medical Device Software Development updates.
When you come to The RND Group, you find people who are just as serious about your work as your own team. We view our clients as collaborators. You’ve worked hard to get your project to this point. We can help take your software across the finish line so you can move your solution to market.
Our specializations cover the entire lifecycle of Medical Device Software Development. We can develop your solution from start to finish, review your existing architecture with a technical assessment, handle your cloud solutions or LIS integrations, and more. No matter where you’re at in your timeline, we’re here to support your vision.
We have a proven process for quality system compliance, as well as a designated in-house team for software verification and validation.
Let us know what your needs are! We are experts in solving Medical Device Software Development problems.
Medical Device Software Development Specifics
- Full lifecycle software development
- FDA CFR Part 820/ISO-13485 compliant quality system
- Engineers average 15+ years of experience
- Requirements analysis, development and management
- Software design, implementation, testing, QA, and verification
- Project management
- Design history file management
- Maintenance and support