FDA-compliant flow cytometry data with the MACSQuantify Software 

  • Automated calibration, compensation, and Express Modes
  • Easy data management
  • Compliance for electronic records and signatures


MACSQuantify Software is available as a stand-alone product or as an additional license for your existing software package.


Calibration and compensation

Automated processes like compensation and calibration ensure consistently high performance. MACSQuant Calibration Beads are specially developed for automated optimization of channel voltage settings. Single stained cells or compensation beads can be used for fully automated compensation on up to eight colors via an 8x8 matrix. See how simple automated fluorescence compensation can be. Watch this video and download the application note.

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Auto-compensation on the MACSQuant Analyzer

It is widely acknowledged that spectral overlap is problematic for flow cytometric analysis using certain fluorochromes. With the MACSQuant Analyzer, 7-color compensation is fully automated. Find out how it can make your life easier!

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Quick guide
Save time with automated compensation on our MACSQuant Analyzers

Download the quick guide on automated compensation and find out how MACSQuant Analyzers can help you save time during your flow cytometry experiments.

Data management

Data files are automatically archived and are easily transferred to hard drive, USB stick, or a network drive. Additionally, all data are stored in a digital format that makes offline compensation easy. Other file formats can be saved as well, including analysis templates (e.g. gating strategies) and FCS files for use by other programs. High-resolution charts can be easily printed or copied for immediate use in presentations or reports.  

MACSQuant Express Modes

Make your life easier with Express Modes. This feature allows you to fully automate and standardize your experimental process. From automated labeling of your sample to the analysis template, everything is done with little effort.

MACSQuantify 21 CFR Part 11 option

Enabling compliance for electronic records and signatures

The Subpart 11 of the Code of Federal Regulations Title 21 (21 CFR Part 11) defines the requirements for submitting electronic records to the FDA as well as the criteria for using electronic signatures. Our optional 21 CFR Part 11 software module of the MACSQuantify Software enables this by:

  • Time-stamped audit trails for all data files, which record the creation, modification and storage of the files
  • Secure password-controlled user login that monitors inactivity time-outs, renewals, and attempted sign-in failures
  • Controlled electronic signatures
  • Optional: Connection to existing LDAP system
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21 CFR Part 11 Statement

Download the 21 CFR Part 11 Statement with detailed information on all MACSQuantify Software features that enable the submission of electronic records to the FDA.


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Quick guide
MACSQuant Express Modes

Find out how to use Express Modes on our MACSQuant Analyzers.

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User manual
MACSQuantify Software 2.11

Find detailed information in the MACSQuantify Software 2.11 user guide.

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