ToxLab 2.0 is a software package specifically designed to handle the data processing needs for drugs of abuse testing, therapeutic drug monitoring, environmental toxicology, and forensic applications.  When used in conjunction with the DSQ II GC/MS system, ToxLab 2.0 offers enhanced automation for these types of analyses, allowing unprecedented productivity, performance, and reliability in toxicological laboratories.

Incorporating real-time unattended injection logic triggered by user defined parameters, ToxLab 2.0 eliminates unnecessary and costly re-injections. Immediately after a sample is processed, ToxLab 2.0 can determine a problem and immediately re-inject a calibrator, QC sample, or autosolvent blank to correct any issue – without operator intervention for true 24/7 productivity.

• Reducing both turn-around time and cost per analysis – Critical for maximizing productivity and profitability
• Minimal user interaction and data review by the analyst and certifying scientist
• Customizable methods and intelligent sequencing to adhere to the laboratory’s standard operating procedure
• Preferred tool when used in concert with the most sensitive GC/MS systems available for today’s successful certified laboratory

ToxLab 2.0 includes several types of reports.  

• Sample Report - The sample report provides quantitation information about each compound in the sample. It shows the integration of the quantitation ion and the qualifying ions. The acceptable or allowable percent range of the qualifying ion ratios is calculated based on the values entered into the processing method and the calculation method that will be used.  Integrations of the quantitation and qualifying ions for the internal standard, along with ion ratios, are also shown. At the bottom of each page will be a pass or fail statement that is based on the ion ratio criteria set in the processing method. Other QA/QC limit reviews are also reported.
• Calibration Report - The calibration report provides a calibration curve and correlation coefficient for each compound. The sample header provides the date and time of the calibration of the method. The level name and raw data file are shown, along with the location of the files when they were used for the calibration.

• Batch Summary Report - The batch summary report provides all integration information for each sample in the sequence. It is a spreadsheet report that shows areas, calculated amounts, and qualifying ion information for each compound along with data review flags.  It will give pass/fail information for each compound in each of the samples. It also provides signature lines for batch review.

  ToxLab 2.0 has been designed to carry out checks automatically and in real time minimizing user input and ensuring that sample batches are not run if QA checks indicate a problem.  ToxLab 2.0 has built-in intelligence and can diagnose certain faults and either try to correct these itself or highlight them to an operator. 

  For example, ToxLab 2.0 will trigger the GC/MS system to inject a blank sample if compounds are determined to be at levels that may produce carryover contamination.  Because the software makes decisions based on data, ToxLab 2.0 provides the analyst with the best possible results.  See a sample of intelligent sequencing below:

  

  ToxLab 2.0 also provides multi-level security access, giving system administrators the freedom to modify user privileges from data review to full system access.  In addition, the software’s audit log records all modifications to the system, ensuring the highest level of data integrity.

  ToxLab 2.0 software, with intelligent sequencing, decreases the amount of time the operator and certifying scientist need to spend with the system. The productivity of the entire system is maximized by ensuring that the batch will be completed with the minimum number of injections or aborted in the event of a curve or QC failure.

  Call 1-800-532-4752 today to set up a demo at our lab or yours!