Laboratory Information Management System

The vendor required to provide laboratory information management system (LIMS) for include:
•    LIMS login access and dashboard
•    Sample receiving
•    Sample preparation  Sample analysis
•    Data review
•    Reporting
•    Sample return and disposal
•    Contract labs
- LIMS login access and dashboard
•    The system will have secure user access with roles and permissions managed by administrators. 
•    It will include password protection, audit tracking, and allow users to log in from any workstation, including remotely. 
•    Users will be able to easily navigate the system through menus and screens. 
•    Administrators can update system settings and monitor activity. 
•    The system will track equipment maintenance and user competency records. 
•    It will also manage inventory of supplies with alerts for low stock and upcoming expirations. lastly, the system will connect with purchase order and procurement processes.
- Sample receiving
•    The system will support electronic and paper test requests, allowing batch entry and linking of requests to samples using barcodes or other tracking methods.
•    It will generate unique accession numbers, create barcode labels, and support instrument-specific data for test batches. 
•    Users will be able to flag sample issues, track chain-of-custody, and record sample conditions such as temperature and humidity. 
•    The system will also support uploading sample photos, automatically reject samples based on custom rules, and allow follow-up tracking for linked samples (e.g., acute and convalescent). 
•    It will manage sample-related reminders, hazard screenings, and partial test entries when full data is not yet available.
- Sample preparation
•    The system will support splitting and aliquoting of samples with proper labeling, and allow routing and tracking of samples across multiple labs, including shipments to reference labs with documentation. 
•    Users will be able to schedule and track each step of sample preparation—such as grinding, homogenization, dilution, and aliquoting—with timestamps and technician ids. 
•    The system will also calculate input mass and dilution factors automatically, ensuring full traceability throughout the preparation process.
- Sample analysis
•    The system will support both manual entry and automated import of instrument results, including raw data parsing. 
•    It will integrate with various instruments and allow real-time management of instrument run queues.
- Reporting
•    The system will generate a wide range of standard and custom reports, including workload, turnaround time, quality control, quality assurance, test logs, and submitter usage. 
•    Reports can be scheduled during off-peak hours, exported in standard formats (e.g., .csv, .xlsx), and delivered automatically via email or a submitter portal. 
•    It will support regulatory reporting, audit-ready QC and QA summaries, and configurable certificates of analysis (COAS) with lab branding and QR code verification. 
•    The system will also track and report on chain-of-custody, CAPA records, and partial batch testing. 
•    Alerts for overdue turnaround times will be included, and users can mark reports as preliminary, final, corrected, or amended.
- Multiple process workflows
•    The system will provide a secure online portal for customers and submitters to enter test requests, track samples, and download reports. 
•    Users will be able to print barcodes and labels before shipping and submit multiple samples in batches with shared information. 
•    The system will support quality control tracking, ensure compliance with industry standards, and provide real-time sample status updates for submitters. 
•    The system will offer advanced search capabilities, enforce data validation and verification, and ensure required fields are completed. 
•    It will support audit trails, electronic signatures, sop versioning, and distinguish between internal and client-ordered tests. 
•    The system will also manage data archiving, regulatory form uploads, and provide real-time and mobile access to sample status tracking. 
•    The system will ensure full traceability by linking reagent lots and test batches to results, track qc measures, and automatically handle retests and batch rejections. 
•    It will provide data analytics dashboards, flag regulatory limit exceedances, and integrate with external tracking systems. 
•    The system will support multi-layered peer and supervisory reviews with audit trails and electronic signatures to maintain quality and compliance.

- Contract Period/Term: 3 years
- Questions/Inquires Deadline: January 2, 2026
- Intent To Bid Form Due Date: January 20, 2026