The Laboratory Information Management System provides management of laboratory information in support of FDA regulated and nonregulated medical research. Further, the EIT PMO coordinates with customers to document their master data. The system manages laboratory data, workflows, and products.
LIMS features modules for:
- Samples and Reagent Lifecycle Management
- Reports, Dashboards, and Labels
- Laboratory execution
- Electronic Laboratory Notebook
- Instrument integration
LIMS is currently used to track the product accountability requirements established by the FDA, as well as tracking investigational products to accurately report product inventory per 21 CFR Part 11.
Features:
- Manage samples through their entire lifespan with end-to-end traceability
- Automate laboratory workflows
- Monitor samples across multiple locations
- Quickly create and maintain laboratory master data
- View key performance indicators at a glance
- Search for data across the system
- Get on-demand reporting and data visualization
- Guide laboratory users step-by-step through tasks
- Track analyst and instrument certifications
- View a workflow's activity history
- Generate and print barcodes for samples
- Track usages, maintenance and calibration of instruments and their parts
Training & Demos
- A variety of training options and demos are available for LIMS.
- If you would like to schedule a demo or training, or have any questions, please contact us.