Scigeniq™ QMS
Our QMS solution provides built-in best practices for CAPA, Change Control, and other quality processes. It ensures compliance with global regulations and quality standards for Life Sciences companies. All investigations, processes, workflows, and quality data are managed in one centralized, flexible system.
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Scigeniq DMS is a complete document management system for managing all your documentation in a secure and compliant manner. It includes complete workflows for document review, approval, modification, release, and discontinuation while maintaining a complete audit trail of all document changes.
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Scigeniq RMS is a comprehensive regulatory management system that tracks and manages all your regulatory submission information and activities. With well-designed structures to organize all correspondence and dossiers, the system can adjust to your specific regulatory activities and ensures complete security while providing access to authorized stakeholders.
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Scigeniq Electronic Batch Records (EBR) automates batch record management, saves time, improves accuracy, and ensures compliance with regulatory requirements. It allows the integration of devices and equipment and collects information throughout the manufacturing process to create a comprehensive batch record, saying goodbye to complex and time-consuming paper-based processes.
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