The system for managing laboratory information must do more than organize data—it must ensure traceability, compliance, and performance under pressure. In most healthcare and research environments, the answer to what is the system for managing laboratory information LIMS software begins with distinguishing between two dominant categories: laboratory information management systems (LIMS) and laboratory information systems (LIS).
Though often confused, LIMS and LIS serve different operational priorities. LIMS platforms are built around specimen-centric workflows. They manage tasks like sample tracking, batch testing, inventory control, reagent usage, and instrument maintenance. LIS platforms, in contrast, are patient-centric and optimized for clinical environments. They handle test orders, result reporting, and seamless integration with electronic health records (EHRs).
Together, these systems form the digital infrastructure drives laboratory operations. They automate repetitive tasks, reduce manual error, enforce standard operating procedures, and support compliance with standards such as CLIA, CAP, ISO 15189, and FDA 21 CFR Part 11. Without this infrastructure, laboratories face greater risk of data loss, delayed results, audit failure, and workflow breakdown.

Selecting the best laboratory information system software requires more than feature comparison. It demands a clear understanding of current lab workflows, reporting requirements, instrument landscape, and scalability goals. The system must also support real-time interfacing, customizable workflows, and robust user access control to protect patient and test data at all stages.
In high-volume diagnostic settings, these systems operate as mission-critical platforms. They ensure every specimen is logged, tested, validated, and reported according to strict internal and regulatory standards. They provide complete visibility into lab performance—from turnaround times and workload distribution to instrument uptime and pending test alerts.
Whether supporting public health surveillance, clinical diagnostics, or specialty research, laboratory operations today depend on reliable, configurable systems designed specifically to manage complex laboratory data.
Laboratory Information System
A laboratory information system (LIS) is the backbone of clinical laboratory operations. Unlike LIMS platforms—which focus on specimen-level workflows—LIS platforms are designed to manage patient-centric processes tied directly to diagnostic testing and result delivery. These systems connect clinical orders, laboratory workflows, and provider communication in a single, compliant, auditable platform.
When exploring laboratory information systems examples, you’ll find widespread deployment in hospitals, health systems, academic medical centers, and commercial diagnostics laboratories. A LIS typically receives test orders electronically from an EHR or manually entered by lab personnel. It assigns a unique identifier to each specimen, ensures proper routing to the correct department, and interfaces directly with analyzers to capture raw results.
The LIS applies validation rules, flags exceptions, and supports technologist review before releasing results back to the clinician. For labs that process thousands of tests daily, this automation ensures both speed and data integrity—key requirements in regulated environments.
Integration is another critical function. A robust LIS communicates bi-directionally with EHRs, billing platforms, quality control systems, and hospital databases. This reduces duplicate data entry, accelerates result delivery, and ensures laboratory data flows consistently across the care continuum. It also maintains audit trails, access controls, and electronic signature capabilities to meet CLIA, CAP, and HIPAA standards.
Examples of LIS usage includes critical care testing where turnaround times are measured in minutes, infectious disease workflows that require reflex testing and public health reporting, and molecular labs needing precise instrument interfacing and result formatting.
Scalability and configurability determine the long-term success of a LIS deployment. The system must be able to accommodate new tests, evolving rules, and departmental growth without requiring full reimplementation. This flexibility separates purpose-built LIS platforms from general-purpose IT systems.
In practice, a LIS is not just a tool—it is a strategic asset. It governs how a laboratory ensures diagnostic accuracy, maintains regulatory compliance, and supports clinical decisions that directly impact patient care outcomes.
LIMS Software
A laboratory information management system (LIMS) is a specimen-centric platform designed to manage non-clinical workflows, complex test protocols, and high-volume sample processing. While the LIS governs patient-facing diagnostics, LIMS software serves as the operational backbone in research, public health, pharmaceutical, environmental, and industrial laboratories.
The core functions of LIMS software include sample tracking, batch processing, reagent and inventory management, instrument calibration, chain-of-custody documentation, and compliance enforcement. Unlike LIS platforms, which align closely with clinical diagnostic workflows, a LIMS is structured to handle configurable workflows not bound to patient-specific data but focused on specimen lifecycle, metadata, and analytical procedures.
LIMS platforms are widely used in labs conducting environmental monitoring, water testing, forensic analysis, vaccine research, and pharmaceutical quality assurance. These environments require detailed data capture, multi-step protocol tracking, and stringent quality controls—tasks LIMS software manages through rule-based automation and system-driven checkpoints.
A key benefit of LIMS software is its ability to enforce standardization across variable testing protocols. Whether managing a stability study in a pharmaceutical lab or a pathogen screening in a public health lab, LIMS ensures every step is documented, time-stamped, and traceable. This not only supports regulatory compliance with agencies like FDA, EPA, and ISO but also improves reproducibility, a key concern in research settings.
Data integration is another strength of LIMS platform. They connect with laboratory instruments, enterprise resource planning (ERP) tools, warehouse management systems, and business intelligence platforms. These integrations eliminate siloed data, reduce manual entry, and improve end-to-end process visibility across lab operations.
LIMS software also supports audit readiness. With built-in controls for user permissions, electronic signatures, and audit trail logging, labs can meet the expectations of auditors and regulatory inspectors without relying on disconnected documentation or manual logs.
In many labs, LIMS operates alongside a LIS—especially when institutions handle both clinical and non-clinical testing. In these hybrid environments, both systems must be properly interfaced and configured to prevent data discrepancies and workflow inefficiencies.
While LIS platforms are optimized for diagnostic precision, LIMS platforms drive operational consistency. Together, they ensure both patient outcomes and laboratory productivity are achieved without compromise.
Choosing the Right LIS
Selecting the right laboratory information system requires alignment with your lab’s testing complexity, integration landscape, and regulatory profile. SCC’s SoftLab® delivers on all fronts—supporting clinical laboratories with high-throughput demands, specialty workflows, and real-time interfacing needs.
The best LIS software provides more than test routing and result reporting. It manages quality control enforcement, rules-based automation, and bi-directional integration with EHRs and instruments—all while maintaining full audit traceability. SoftLab supports enterprise-scale operations without sacrificing performance or configurability, making it a trusted solution across leading healthcare networks. For labs prioritizing diagnostic speed, regulatory accuracy, and long-term scalability, SoftLab remains the benchmark for LIS performance and reliability.