Thermo Scientific LCQUAN Quantitative Software

21 CFR Part 11-compliant software for quantitative LC-MS/MS data acquisition and management

Thermo Scientific™ LCQUAN™ quantitative software is a robust, regulatory-compliant data system tailored for bioanalytical laboratories conducting LC-MS/MS assays. Developed in close collaboration with pharmaceutical industry experts, LCQUAN provides all the tools needed to acquire, process, review, and securely manage quantitative data across global drug development workflows.

Key Features

Regulatory Compliance

• Fully compliant with FDA 21 CFR Part 11 requirements for electronic records and signatures
• Enables secure submission of electronic documents to regulatory agencies, including the FDA

Comprehensive Workflow

• Guides users step-by-step through acquisition, method development, data review, processing, reporting, and export
• Supports import of sequence information from external systems
• Streamlines interaction with Thermo Scientific™ Watson LIMS™ for GLP-compliant bioanalytical studies

Secure Data Management

• Enables data processing on networked systems, including secure remote disks
• Centralized, workbook-style data storage for easy archiving and retrieval
• Multi-level user privileges—from full system access to read-only modes

Seamless LIMS Integration

• Bi-directional communication with Watson LIMS facilitates study tracking, chromatogram review, auditing, and compliance
• Optimized for regulated pharmaceutical workflows from discovery through clinical trials

Proven Platform

• Part of an integrated Thermo Scientific LC-MS/MS solution suite, including TSQ Series mass spectrometers and FAIMS interface technology
• Ensures high sensitivity, robustness, and reproducibility for regulated bioanalytical assays