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diaLIMS

Laboratory data management and sample tracking for analytics, quality assurance, and R&D with automated workflows and regulatory compliance.

Overview

diaLIMS is an industry-independent, standard laboratory information management system (LIMS) developed by dialog EDV, designed to support the digitalisation of laboratory processes across analytics, quality assurance, and research & development. Built on a flexible core system, diaLIMS goes far beyond classic LIMS functionality, offering comprehensive data management, process documentation, and compliance capabilities suitable for laboratories of all sizes and sectors.

The platform is modular and highly customisable, enabling laboratories to tailor the system to their specific workflows. It covers the full sample lifecycle, integrates with analytical instruments and third-party systems, and supports regulatory compliance across a wide range of international standards.

Core Features and Capabilities

  • Customer Relationship Management (CRM) for managing laboratory clients and orders
  • Sampling planning and on-site sampling support
  • End-to-end sample management and control
  • Manual and automated data acquisition from analysers and connected systems
  • Analytical quality assurance (AQA) tools
  • Reporting, analyses, and statistical evaluation
  • Sector-specific quality assurance for industry
  • Quality management support

Sampling Management

  • Comprehensive planning, execution, and documentation of sampling activities
  • Tools to efficiently determine sampling locations and manage sampling appointments
  • Mobile sampling support via a dedicated diaLIMS sampling app for field use

Sample Management Workflow

  • Guides samples through the entire laboratory process, from receipt to finalisation
  • Records incoming samples and orders in compliance with relevant standards and guidelines
  • Creates worklists, assigns measured values, and checks limit values automatically
  • Mobile app support for accessing stock information and managing sample releases on the move

Interfaces and Measured Value Acquisition

  • Flexible connection to analysers, third-party systems, and standard interfaces
  • Automates the transfer of measured values and management of laboratory data
  • Workstation- and method-specific measured value recording
  • Optional automatic import of measured values from analysers
  • Automatic limit value validation

Test Equipment Management and Analytical Quality Assurance

  • Monitors and manages test equipment and analysers
  • Tracks testing schedules and maintenance requirements for instruments
  • Automatic generation of worklists for equipment checks
  • Flexible device connection and regular result verification following equipment checks

Reporting and Evaluation

  • Automatic generation of reports, analyses, and statistics directly within the system
  • Template-based reporting for convenient and consistent output
  • Creation of standard-compliant test reports in accordance with ISO 17025

Additional Modules

  • Warehouse management
  • Legionella assessment
  • Chemicals management
  • Management of hazardous substance and dangerous goods information
  • SampleTray visualisation

diaLIMS is compliant with a broad range of regulatory frameworks including GLP, GMP, ISO 9001, ISO 17025, FDA 21 CFR Part 11, GDPR, IFS, and WADA. An internal audit trail ensures full traceability of all changes and versions throughout the system. The software can be presented on-site or via remote demonstration, and the dialog EDV team provides direct customer support for implementation enquiries.

Meta

Domain
Lab Informatics & Operations
Subdomain
Laboratory Information Management System (LIMS)
Software type(s)
Record-Keeping System
Deployment type(s)
Hybrid
Industry vertical(s)
Academic / ResearchBiotechDiagnostics / IVDEnvironmental / Food SciencePharma
Development stage(s)
ManufacturingPreclinical / Pre-MarketResearch & Discovery
Target user(s)
Bench Scientist / Lab TechnicianLab Manager / Core Facility ManagerResearch ScientistQA / Regulatory Affairs
Compliance standard(s)
21 CFR Part 11GxPGDPRISO 27001