AIVIS
NON CDS

Pharmaceutical laboratories often rely on multiple analytical instruments, many of which do not offer seamless integration or automated data management capabilities. This creates silos of information, manual review processes, and greater risk of oversight in compliance-critical operations.

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AIVIS bridges this gap by enabling intelligent audit trail review and data monitoring for non-chromatographic systems. It standardizes review processes, enhances traceability, and provides meaningful visibility across diverse laboratory instruments — all within a unified, digital environment.

 

The platform simplifies how laboratories monitor critical events, manage review workflows, and ensure compliance with regulatory expectations. By automating routine checks and consolidating key information, it reduces manual effort while improving accuracy and accountability.

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Through AIVIS, organizations gain a centralized, efficient, and compliant framework for managing non-chromatographic instrument data — ensuring every part of the lab contributes to a connected, integrity-driven ecosystem.