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Creating a Product Quality Review (PQR) can be challenging for pharmaceutical companies. The process involves gathering and analyzing vast amounts of data from various sources, ensuring all information is accurate and up-to-date. This can be time-consuming and prone to errors, leading to compliance issues and inefficiencies. Management and QA professionals often struggle to maintain consistency and accuracy in PQR generation, impacting decision-making and operational effectiveness.
QEdge PQR is the ultimate solution for seamless and efficient Product Quality Review creation in the pharmaceutical industry. Our software simplifies the PQR process by integrating existing systems, automating data collection, and ensuring accuracy and compliance.
QEdge collects data from various sources, including electronic Batch Manufacturing Records (eBMR), Laboratory Information Management Systems (LIMS), electronic Quality Management Systems (eQMS), ERP/SAP systems as well as manual Excel sheets. The software integrates this data seamlessly, performing automated analysis and graph plotting. The resulting PQR report is detailed and comprehensive, providing clear insights into product quality and compliance metrics.
