The increasing complexity and stringency of safety and quality standards required in today's medical device industry make the development and integration of these systems crucial. Foliage has helped many clients design, develop, and integrate a wide variety of complex software intensive products enabling medical device companies the freedom to focus on the clinical components and business tasks that are their core areas of competency.
Foliage has deep experience with the development standards and processes that comply with the FDA's 510(k) requirements as well as industry standards such as DICOM and HL7. Partner with Foliage to:
- Product assessments (strategy, architecture, process, test automation)
- Product line planning
- Risk management
- Software and system architecture and design
- Requirements management
- Project planning and management
- Process planning and management
- Software and system development
- System integration
- Testing and test automation
Foliage's combination of packaged and custom services can eliminate your specific medical device product development challenges while you focus on the science behind building innovative products.
