Sample Management Solutions for Applications
From cell lines to small & large molecules and lab integration - find out why Xavo is always the right decision!
Cell Line Management
Xavo revolutionizes cell line tracking and maintenance by providing a centralized, automated system for monitoring cell provenance, culture conditions, and experimental usage. It ensures that every cell line is correctly labeled, stored under optimal conditions, and retrieved without errors—eliminating mix-ups and maintaining research reproducibility.
For pharmaceutical, biotech, and academic labs, compliance with industry standards is essential. A secure digital audit trail allows researchers to track passage numbers, freeze-thaw cycles, and genetic modifications, ensuring full regulatory adherence and scientific integrity.
By integrating AI-powered automation and real-time monitoring, Xavo helps researchers enhance efficiency, ensure data accuracy, and streamline workflows, allowing them to focus on innovation and discovery rather than manual record-keeping.
Small Molecules
Xavo streamlines small molecule tracking and lifecycle management, ensuring that every compound is accurately labeled, stored, and accessed with full traceability. By automating inventory control, expiration monitoring, and experimental usage tracking, labs can reduce errors, optimize workflows, and improve efficiency.
Regulatory adherence is another critical factor. A digital audit trail ensures that every step—from synthesis to assay screening and formulation—is recorded and audit-ready for regulatory inspections.
With AI-powered automation and real-time monitoring, Xavo helps research teams maximize efficiency, ensure data accuracy, and maintain full compliance, allowing scientists to focus on drug innovation rather than administrative burdens.
Large Molecules
Xavo ensures full traceability and lifecycle management of large molecules by automating storage conditions, concentration tracking, and aliquoting processes. This prevents errors in formulation, ensures batch-to-batch consistency, and helps maintain the integrity of oligomer-based therapeutics.
Compliance is another key challenge. A digital audit trail provides complete transparency, reducing the risk of regulatory delays.
Additionally, AI-powered automation enhances efficiency by integrating real-time monitoring, expiration tracking, and inventory management, enabling researchers to optimize workflows, reduce errors, and accelerate the path to clinical and commercial applications.