Advanced spectroscopy software for quality assurance and quality control

Horizon QA software

This modern software provides superior ease of use and includes a full-featured operator interface.

Overview
Data
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Overview

QA Applications version

The Horizon QA software replaces the AIRS platform in the Horizon MB Software Suite for QA/QC applications. This software includes multiple improvements and expands the functionalities to support legacy of the former FTLA platform and full instrument validations for the MB3000 and FTLA series. 

Horizon QA
























What’s in the Horizon
QA
  • Support of legacy instrument (FTLA) platform
  • Full instrument validation
  • Pre-configured workflow with sequential data acquisition, analysis, and reporting
  • Makes routine analysis of physical and chemical properties easy and eliminates operator errors
  • Configurable settings allowing extensive customization
  • Comprehensive status display for concentrations and analysis history
  • Complete reporting solution
  • Support chemometric options including peak height/area, Horizon Quantify, PLSplusIQ, Grams IQ, SIMCA P+ and Unscrambler
  • Real time analyzer health monitoring
  • Intelligent tools for data export, and archiving

 

 

 

Data

Advanced spectroscopy software for quality assurance and quality control compliant with CFR 21 part 11 environments.

Facilitating Qualitative and Quantitative Analysis providing secure and efficient analysis.

Features and Benefits
− Pre-configured workflow with sequential data acquisition, analysis, and reporting
− Makes routine analysis of physical and chemical properties easy and eliminates operator errors
− Configurable for Batch Mode operations
− Configurable settings allow extensive customization including user defined messages that can be written in any language
− Comprehensive status display for concentrations and analysis history
− Complete reporting solution
− Support chemometric options including peak height/area, Horizon MBTM Quantify, PLSplusIQ, GRAMS-IQ, SIMCA P+, and Unscrambler models
− Extensive diagnostics and real time analyzer health monitoring to track the status of the analyzer
− I ntelligent tools for data export and archiving
− Usable in 21 CFR part 11 compliant mode and in other regulated environments.

Validations
Numerous validation routines integrated in the software verify that your instrument is operating as it should. Validation can be performed in accordance with ASTM and/or Pharmacopeia protocols. 

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