Faster. Smarter.
Medical Software and AI
Navigating the complexities of regulated industries so you can focus on innovation.
Innovira Consulting provides expert software and AI guidance for FDA/MDR quality, HIPAA/SOC2 compliance, and successful product launches.
From concept to market
Services
Regulatory Compliance
Navigating the regulatory landscape can be daunting. Innovira streamlines the 510(k) submission process for medical device companies, ensuring compliant engineering documentation and efficient regulatory pathways. HIPAA compliance and SOC2 certification comes standard for a complete solution
Software Development
Medical software has extra contingencies that can be complex. Innovira offers end-to-end software development and support for medical devices, including mobile app development, backend infrastructure, cloud deployment (AWS). Automated regulatory documentation comes standard
AI Development
AI in medical software can be complex. Innovira provides comprehensive guidance through the entire process. Whether building deep learning or machine learning models, or implementing computer vision, Innovira has you covered.
Engineering Leadership
Startups and smaller companies that may not need a full-time CTO. Innovira provides fractional CTO and VPE services. For investors and companies seeking an independent assessment of their technology stack, regulatory compliance, or product potential, Innovira provides technical due diligence and product assessment.
Schedule a complimentary consultation
Schedule your consultation today to leverage our expert insights and drive your business forward. Innovira is ready to provide tailored solutions to meet your organization's unique needs.
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