Integrated knowledge and risk management
for compliant device development and commercialization
Leverage our expertise in advanced visualization and digital knowledge management to optimize innovation, reliability, and compliance in your device development and commercialization.
Achieve deeper knowledge retention and stimulate innovation using digital cloud-based knowledge management systems for seamless real-time collaboration.
Enable rapid knowledge collection and distribution through our visual-digital manufacturing execution systems (MES) and electronic quality management systems, enhancing compliance, traceability, and optimized device performance.
Our team combines a visual-digital investigation approach with extensive medical device development experience to use your knowledge and quality risk experience to permanently address the root causes of quality issues and complaints.
Learn more about Minerva’s C3 technical investigations and R3 quality investigations here.
Comprehensive risk assessment frameworks to identify, evaluate, and mitigate potential failures
—including software risks— to ensure reliable and compliant device development, manufacturing, and usage.
Risk-based process optimization through mapping, visualization, and integrated risk files for successful process verification and validation.
Transforming the medical devices industry through visual-digital knowledge and quality risk management.
