QX Manager Software, Regulatory Edition #12012172



QX200 System Control and Analysis Software, with traceablity for secure environments



Use QX Manager Software Regulatory Edition, to assist in compliance with U.S. FDA 21 CFR Part 11 regulations when performing PCR experiments on the QX200 and QX200 AutoDG Systems.

QX Manager Regulatory Edition works in conjunction with the built-in security features of the Microsoft Windows 10 operating system to provide a security environment for the maintenance, verification, and tracking of all electronic records generated by the software. When properly configured and administered, these tools ensure compliance with the rules for secure handling of electronic records as outlined in Title 21, Part 11 of the Code of Federal Regulations (CFR).

Key Features

  • Streamlined workflow system control and analysis
  • Easy Plate Set up with multiple descriptor fields for sample names, well notes, and plate notes
  • Supports simple to advance analysis for all experiment types and plex modes experiment
  • Customizable data handling and report generation

Key Security Features:

  • Mandatory password-protected log-in — log-in required; administrator sets user privileges
  • Time- and date-stamped audit trails — edit information is tracked and saved. Audit trail records reason for save and option to export as PDF report
  • Lot management tool — document consumable and reagents lot information
  • Electronic signatures — multiple electronic signatures can be applied at any editing step

Download the instruction manual to learn more about QX Manager Software, Regulatory Edition and the QX200 Droplet Digital PCR System.

Product Contents

  • QX Manager Software Regulatory Edition
  • USB license key

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