L7|ESP gives diagnostic companies total visibility over all their operations while digitizing, integrating, and automating scientific, analytical, and operational workflows. L7|ESP will increase sample throughput and quality assurance in results and provide reliable documentation for regulatory review (CAP/CLIA/GLP/cGMP). L7|ESP automates the entire sample to report process including sample and order management, barcode scanning, bio-repository management, lab data collection and analysis, data visualization, integration to all instruments, automated clinical report generation, e-signatures, and electronic delivery of reports to providers. The L7|ESP platform provides out-of-the-box apps, including ELN, LIMS, inventory, assets, location, analysis, data, projects, dashboards, reports, e-signatures, etc.
precision diagnostic workflow
legacy data and process silos continue to exist hinders efficiency and science, increases risk for business and patient
L7|ESP helps you achieve operational excellence by increasing sample throughput and providing better reproducibility while being a fully integrated and automated process (e.g., NGS workflow).
Our platform is able to provide reliable and easily accessible data documentation to facilitate accurate submissions for regulatory approvals.
solution data sheet
POSTED ON January 1, 2020
BREAKING DOWN DATA SILOS IN THE LAB; HOW INTEGRATED DATA MANAGEMENT SYSTEMS CAN SUPPORT DIAGNOSTIC LABS
L7|ESP provides complete end-to-end assay automation and is designed to increase reproducibility and efficiency while decreasing errors and turnaround time.