We function as an extension of your team.
- Do you want to partner with a firm that specializes in Requirements Management for software for medical devices?
- Do you want to partner with a firm that specializes in designing/developing software following our 13485 compliant Quality System with the FDA in mind for medical devices?
- Do you want to partner with a firm that specializes in managing and developing projects on time within budget?
RND’s capabilites center around our expertise of understanding your requirements. RND has been developing software for the medical device industry for over 15 years. We have the expertise to ask the right questions to help draw out the requirements necessary to engineer your software. If your requirements are clearly understood, it makes the task of managing the full lifecyle project based on our mature quality system to deliver the software on time and within budget.
- FDA Part 820, Part 11
- ISO 13485, HIPAA, IEC 62304
- Software Lifecycle
- Windows Development
- Mobile Development
- Embedded Development
- Mac Development
- Requirements Management
- Project Management
- Software Verification