Enabling a digital quality ecosystem to deliver the promise of proactive quality
End-to-end solution for enterprise quality management
The world’s first AI-enabled platform designed to augment quality management decision-making
Combine modular visualization, MES, and batch historian to digitalize, orchestrate, and optimize production for Life Sciences
Providing contextualized data history without complex rules configuration
Go paperless, enable compliance and accelerate digital transformation
A library of business applications, each designed to meet a specific life sciences use case
Transforming the Quality Management Review Process
Modernize the Annual Product Quality Review (APQR) process
Our QPAs are intelligent, pre-validated quality processes that are built on almost three decades of industry best practices and help shorten time to value.
The complaint handling QPA provides the ability to log, respond to and investigate complaints.
The supplier quality management QPA enables organizations to manage and collaborate with suppliers and contract manufacturers across your supply chain.
Risk Management enables companies to seamlessly link the risk process to other quality management processes.
The audit management QPA helps companies monitor critical processes, identify gaps and improve quality.
The CAPA QPA enables organizations to track and manage the process of carrying out CAPA plans, automate verification of effectiveness over time, and provide seamless traceability to related quality processes, including change control and training.
The nonconformance QPA records data about situations in which a product or device has not conformed to standards.
Access, edit, approve, store and share the latest version of quality documents throughout the value chain
With training management, automate company-wide training policies and regulatory requirements, where training activities are scheduled and tracked through completion
Document and track results of in-process or finished product testing falling out of specified limits using the Out of Specification (OOS) QPA.
The change management QPA manages change at every level of the supply chain to ensure quality and compliance requirements are not affected.
Respond to adverse events faster with the quality events QPA and reduce the amount of time it takes to act on quality and safety issues.