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As the control center for your vitro diagnostic medical device mass spectrometer, Analyst MD software provides advanced performance and features that are faster and more efficient software solution than any other clinical diagnostic software platforms. With Analyst MD software, experience:
Experience a new level of robustness with our intuitive software for medical device that offers simple, flexible and fast data acquisition and reporting on your in vitro diagnostic medical device mass spectrometers.
You’re in control
Analyst MD software delivers full-system integration and enables LC and MS method development, all from a single point of control. Additionally, Analyst MD software acts as the central integration software platform for add-on packages such as MultiQuant and Cliquid MS software, providing you with additional analysis and processing options.
Screen, verify and quantify with confidence
Spend more time understanding your data and less time running your samples. Analyst MD software was designed to maximize the performance of your LC-MS/MS system so you can acquire data with high accuracy and precision. Easily schedule up to 4000 individual MRM transitions within a single run with Scheduled MRM™ Algorithm Pro so you can detect and quantify analytes with confidence.
Reveal hidden compounds, instantly
Don’t wait to uncover underlying peaks. The Dynamic Background Subtraction (DBS) algorithm allows you to subtract background ions and uncover underlying analytes dynamically throughout a run.
Quality with less effort
Forget the endless scrolls through each chromatogram to view your peaks. With the integration quality index, you get instant information with less information. Our unique hybrid QTRAP technology enables you to obtain quantitative and qualitative information in the form of structural information in a single injection using the Information-Dependent Acquisition (IDA) mode, providing you added confidence for your most challenging assays.
Compliance at heart
Analyst MD software makes compliance less cumbersome, incorporating comprehensive security and audit trail features and functionalities that provide the documentation and electronic records required for GLP compliance. Maintain your laboratory standards by relying on Analyst MD software, designed to support 21 CFR Part 11 compliance regulations.
Unveil the benefits of mass spectrometry for your most challenging clinical assays with our portfolio of robust and sensitive LC-MS/MS solutions registered as Class I and Class A in vitro diagnostic medical device under FDA and IVD-R, respectively.
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