Today, many manufacturers’ have quality management systems that only address quality at a functional level, not enterprise-wide. The result is no full end-to-end visibility of issues or common use of best practices to optimize quality and quality processes across the organization. ENOVIA Quality Management provides an effective and efficient quality management system to enforce common quality processes, support global and local regulatory requirements and manage all quality events, such as corrective and preventive actions (CAPA), product nonconformance, and audits, across the enterprise.
In many industries, such as Healthcare and Life Sciences, ensuring regulatory compliance is business critical. ENOVIA Compliance Management helps ensure proper product approvals and certificates in support of business sustainability as well as product safety and effectiveness.
Global operating companies must ensure materials compliance to regional environmental directives. With ENOVIA Compliance Management, compliance managers can implement a well-defined process for requesting, reviewing, and approving materials compliance. Product compliance can be assessed and documented to meet material regulations.
Extend compliance data to a broader audience, allowing for more effective decisions and awareness
Integrate supplier declarations early into the product development
Design in material compliance and monitor in real-time
Establish end-to-end traceability during the development process that can be leveraged for impact analysis