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In today’s fast-paced pharmaceutical industry, manual data collection and reporting processes are no longer sufficient to keep up with regulatory demands and internal quality objectives. Companies need a robust, automated solution to manage large volumes of quality data and generate real-time trend reports. QEdge addresses these needs by providing a centralised platform that eliminates the inefficiencies of manual reporting, improves data accuracy, and ensures compliance with stringent regulatory requirements (USFDA, EMA, WHO).
Automated trend reports reduced report generation time from weeks to minutes, allowing quality teams to focus on improvement initiatives.
Automated integration and validation
minimized manual
data entry
errors.
Real-time trend analysis enabled prompt addressing of nonconformities, reducing the risk of quality deviations and audit findings.
Auditors could access both historical and real-time trend data, improving readiness for regulatory inspections and reducing compliance risks.
QEdge integrates quality data from multiple sources into a centralized platform, automating the process of report generation and trend analysis. This allows the company to monitor key quality metrics in real time via customizable dashboards. The system is designed to meet global regulatory standards, providing continuous compliance monitoring and ensuring the company is always audit-ready.
Report generation time decreased from weeks to minutes.
Data integrity was ensured through automation, reducing errors.
Real-time analysis allowed for faster identification and resolution of quality issues.
Automated reports improved regulatory compliance, reducing the risks during inspections and audits.
QEdge Quality Management Software Suite
Contact Us
6th Floor, Arista, 100 Feet Anand Nagar Rd, Jodhpur Village, Ahmedabad, Gujarat 380015
Phone : +91-79-66214899
Email: sarjen@sarjen.com