Your Complete Solution for Quality Management Excellence
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, batch historian, DCS and more to digitalize, orchestrate, and optimize production for Life Sciences
A Modular, Scalable Manufacturing Execution System (MES)
Providing contextualized data history without complex rules configuration
Go paperless, enable compliance and accelerate digital transformation
A Comprehensive DCS for Automating and Visualizing Batch Production
Transforming the Quality Management Review Process
Modernize the Annual Product Quality Review (APQR) process
Streamlining the Recall Management Process
Modernize the Annual Product Quality Review Process
The annual product quality review (APQR) process is a requirement for manufacturers of drug products to comply with Good Manufacturing Practice (GMP) regulations and maintain high-quality products. However, data aggregation tasks and siloed analysis can plague APQR preparation often hindering product quality decisions, leading to inefficiencies and errors in the process.
Streamline the creation of APQR reports with the TrackWise PQR app. Say goodbye to burdensome manual efforts and embrace a streamlined process that enhances collaboration, improves operational efficiency and meets regulatory compliance. Experience the future of APQR reporting with TrackWise Product Quality Review.
TrackWise PQR enables users to quickly access and analyze data from multiple systems, reducing manual errors and redundancy. Automating data collection and analysis enhances operational efficiency while maintaining data integrity.
By simplifying and automating the process, users can create virtual or interim PQRs, allowing them to routinely assess the state of their processes and review the progress of their continuous improvement initiatives.
TrackWise PQR allows users to automate complex analysis of quality data and collaborate seamlessly across departments. Real-time collaboration ensures swift identification and resolution of product quality issues.
By applying the latest digital technology to automate the process end-to-end, drug manufacturers can streamline their data collection, analysis, collaboration and approval processes. This supports increased operational efficiencies, improved regulatory compliance and reduced costs.
Download the whitepaper to learn how automating the APQR process can help simplify your product quality review process and help you make informed product quality decisions quicker and on a more routine basis.