Developing Safe, Effective Medical Device Software
Genova Technologies’ teams and developers can step in at any stage of your Software Development Lifecycle (SDLC) to help your experts develop safe, effective, and FDA / IEC 62304 compliant medical device products and applications. We are a true Engineering Services company, working closely with you and your team to understand every aspect of your design, development, and testing needs, to help ensure quality Class I, II, and III medical device products and applications.
CUSTOM SOFTWARE & MOBILE APPLICATION DEVELOPMENT
As patient care increases in intricacy, medical device software development becomes more complex as well. Now more than ever, you need a trusted and experienced partner who can help you through every step of your software development process.
Genova’s U.S.-based, full-time engineering team has a wealth of experience, and their focus is on ensuring the job is done right the first time. Genova helps you determine your software level of concern, ensure your software is 100% safe, and that it meets or exceeds all regulatory requirements.
Whether serving as your full-time development team, or aiding your current team, our staff keeps you up to date, informed, and involved in every step along the way. We provide support and partnership to improve efficiency throughout the software development process, leveraging best practices and tools to manage risk and stay on schedule.
EXPERIENCED AND RELIABLE
As medical devices become increasingly complex, you need a reliable partner for your software projects.
Hardware engineering and concept design is often the strength of many medical devices development companies. Oftentimes though, it’s more efficient to delegate software development and processes to trusted partners for cost-effective execution.
At Genova, our expert engineers have designed software and applications for electronic and electromechanical systems, with performance, reliability, cost, manufacturing, and regulatory compliance in mind. Our experienced software developers, engineers, and testers offer specialized skills and abilities for a wide range of advanced electronic and electromechanical device projects.
Genova is ISO 13485 compliant, and its quality systems and practices are compliant with standards IEC 62304, ISO 14971, 93/42/EEC, and CMMI Level 3.
Genova Technologies can help you with any step in the medical device software development lifecycle process, including:
• Full software life-cycle development
• Software verification and validation testing
• Design History File (DHF) Remediation
• Independent medical systems verification/validation to support your submissions
• Unit module testing and integration testing (Black box-White box)
• Waterfall or Agile Scrum processes; including Certified Product Owners and ScrumMasters
• Algorithm development
• Mobile Application Integration
Explore Medical Devices
Software Languages, Tools, & Processes
Genova can provide individual or team experts in a variety of language platforms.
Custom Application Design, Development and Support
Genova designs and develops software applications for commercial, education, government, and medical & health customers, utilizing embedded, application, mobile, web and cloud technologies.
Software Verification & Validation
Genova’s process employs rigorous CMMI methodologies for evaluating the correctness and quality of software products throughout the software life cycle, ensuring that the outcome and work product of a project meets formal specifications, for a variety of “Safety of Flight” and “Safety of Life” applications.
4250 River Center Ct NE, Cedar Rapids, IA 52402
Monday Through Friday 8:00 AM – 4:30 PM
Due to COVID-19, building access or business hours may be restricted. Please call before visiting the office.