A Secure Clinical Laboratory Platform

A multi-tenant, NEHR-aligned platform that brings together LIS and LIMS capabilities to support modern clinical laboratories with traceability, secure data governance, and integration readiness.

About eLizSystems

eLizSystems is a unified clinical laboratory platform that brings together LIS and LIMS capabilities to support routine diagnostics and advanced workflows within a single configurable system.

The platform is designed to support clinical laboratory operations, multi-site and satellite environments, and secure SaaS deployment models aligned with healthcare data protection and regulatory requirements.

Built with structured audit logging, role-based access control, and secure integration capabilities, eLiz enables laboratories to manage operational workflows while maintaining control, traceability, and data integrity.

Built for Operational Control and Traceability

Patient-to-Report
Traceability

End-to-end traceability from patient registration through to final result reporting

Multi-Site
Laboratory Support

Designed to support coordinated workflows across multiple laboratory sites and networks

Workflow and
Validation Control

Configurable workflow and multi-level validation steps to ensure controlled result processing

Instrument Integration
Framework

Supports connectivity with laboratory instruments for automated data capture and workflow efficiency

Secure
API-Based Integration

Enables secure integration with external systems through standardised API-based interfaces

Cloud-Native
Deployment

Designed for scalable, multi-tenant SaaS deployment with flexible hosting options

Comprehensive
Audit Logging

Structured audit trails across system activities, validation steps, and operational workflows

Designed for

// Clinical Diagnostic Laboratories
// Molecular & Genomics Laboratories
// Clinical Research Laboratories
// Private Laboratory Networks
// Multi-Site Laboratory Operations
Configured for routine diagnostics, advanced workflows, and scalable laboratory operations.
A diagram illustrating core platform capabilities with a central circle labeled 'Core Platform Capabilities' surrounded by eight features, including patient-to-report traceability, comprehensive audit logging, cloud-native deployment, secure API-based integration, multi-site laboratory support, workflow and validation steps, instrument integration framework.

End-to-End Laboratory Workflow

1

Collection & Accessioning

Supports batch collection and accessioning workflows, including the capture of consent and test request documentation. The platform can integrate with ordering systems and external hosts to enable efficient and standardised sample registration.

2

Analytical Processing

Supports generation of specimen identifiers (SID) and specimen labels to enable accurate tracking across pre-analytical and analytical workflows.

The platform supports both manual and automated processing, with configurable technical worksheets to capture and manage analytical steps within the LIS. This supports auditability, traceability, and centralised record management for laboratory operations.

3

Validation

Supports critical result flagging and structured multi-level validation workflows, covering both technical and clinical validation stages.

Electronic signature controls aligned with 21 CFR Part 11 requirements are supported, with role-based review and configurable escalation to higher approval levels to ensure controlled, traceable, and clinically safe result validation.

4

Reporting

Provides configurable report template management to support standardised reporting across laboratory operations.

Supports multilingual reporting (including English and Chinese), with parameterisation of report layouts, logos, and templates based on test lines and reporting requirements.

Platform Capabilities & Trust

Platform Capabilities

Laboratory Workflow Management

Result Validation & Reporting

Instrument & System Integration

Audit & Traceability

Multi-Site Operations

Built for Secure Healthcare Environments

Secure system architecture

Audit and traceability

Managed SaaS deployment with local hosting options

Interoperability with healthcare systems

Designed for healthcare workflows

Compliance Focus

Designed with consideration for:

Singapore NEHR submission requirements

Ensures strict compliance with NEHR submission standards by validating data formats, security requirements, and regulatory rules before submission.

PDPA-aligned data handling practices

Enforces PDPA-aligned data handling to safeguard personal information and maintain regulatory compliance.

Secure transmission and audit traceability

Provides encrypted data transmission and complete audit trails to ensure security and traceability.