Engineering Domain : Product Life Cycle Management Prerequisites : CPF MatrixOne 10 | PRG MatrixOne 10 Available since : ,
The process of dealing with Quality issues, such as Corrective and Preventative Actions (CAPA) and product complaints, is the single greatest source of regulatory risk for Life Sciences companies today. The process gets bogged down with all of the documentation and fails to adequately address the critical issues regarding risk, root cause and remediation. Life Sciences companies consistently struggle to deal with Quality issues effieciently and effectively. And as the complexity of products and processes increases, this predicament only promises to worsen. Meanwhile, Life Sciences companies are not getting the strategic value they should from the vast resource of valuable feedback collected in their Quality systems. The ENOVIA Life Sciences Accelerator for Quality Issues provides Life Sciences companies the abillty to effectively and efficiently manage Quality issues by improving QSR/GMP/ISO compliance while eliminating non-value-added waste. The ENOVIA Life Sciences Accelerator for Quality Issues manages all Quality issues through a single, global, on-line system to provide insight into the health of your CAPA processes.
Provides a ready-to-use business process for managing Quality issues such as CAPA and product complaints.
Interacts seamlessly between the CAPA process and other PLM business processes such as change control, product development, supplier control and others.
Ensures that your business process is properly executed and all critcal requirements are met leading to greater regulatory compliance.
Automates the routine aspects of your Quality investigations, reducing waste and focusing attention on the truly critical issues of risk, root cause and remediation.