Built for People Who Review LC-MS Runs Every Day
LC/MS-IQ was created to solve a common laboratory problem: daily LC-MS review often depends on spreadsheets, manual checks, memory, and inconsistent review habits.
The goal is simple: help laboratories review calibration, QC, unknown samples, and analyte health in a clearer, faster, and more consistent way.
Why LC-MS-IQ Exists
LC-MS laboratories generate a large amount of review data from every run. Calibration points, QC levels, peak quality, retention time, signal-to-noise, internal standards, unknown readiness, and historical trends all matter.
LC-MS-IQ organizes that information into a structured review layer so laboratories can focus on the analytes and injections that need attention instead of manually hunting through exports and spreadsheets.
Real LC-MS Laboratory Experience
LC-MS-IQ was developed from practical experience with clinical LC-MS/MS workflows, method development, validation, troubleshooting, automation, and laboratory operations.
Clinical LC-MS/MS
Hormones, toxicology, amino acids, therapeutic drug monitoring, newborn screening, and related workflows.
Daily Operations
Run review, troubleshooting, quality monitoring, staff workflow, and high-throughput laboratory decisions.
Quality Systems
Calibration, QC review, method acceptance criteria, trend monitoring, and documentation.