LabHQ LIMS - 2026 Pricing, Features, Reviews & Alternatives

LabHQ LIMS is a laboratory information management system designed for quality control laboratories in regulated and non-regulated industries. The system provides comprehensive sample and lab management capabilities to streamline quality assurance and quality control operations. Since launch in two thousand twelve, LabHQ has served laboratories of varied size across sectors such as pharmaceutical, agriculture, manufacturing, chemicals and petrochemicals, food and beverage, textiles, contract testing and cannabis analysis. A development team with decades of quality control and Good Laboratory Practice experience in regulated settings underpins the system design to support environments where compliance and data integrity are essential.

The system offers a comprehensive set of functionalities for sample and data management, workflow and workload management, and analysis and reporting. Laboratories can monitor performance indicators and service level agreements while reducing sample turnaround times, increasing throughput and identifying workflow bottlenecks. Workflow tools enforce consistent sample processing protocols while optimizing operations, team performance and resource allocation in real time. The reporting module enables generation of certificates of analysis, automated reports and trend analyses in a few steps to support data-led decision making. The system also incorporates equipment management and an external user portal to facilitate collaboration and transparency among stakeholders. A security framework with bank-grade protection, data encryption, user authentication and version control safeguards data integrity and regulatory compliance.

LabHQ integrates with key regulatory frameworks and compliance standards that laboratories rely on. The system supports adherence to ISO nine thousand one quality management and ISO seventeen thousand twenty-five testing and calibration requirements. It aligns with Health Products Regulatory Authority standards, Medicines and Healthcare products Regulatory Agency guidelines and Health Insurance Portability and Accountability Act protections for data safety. Support for Good Manufacturing Practices and Good Laboratory Practices is provided through quality control workflows, clear documentation and consistent data management. The solution also maintains secure, trackable electronic records and signatures in line with FDA twenty-one Code of Federal Regulations Part eleven.