Our eShop is currently on maintenance and therefore only available with limited functionality. Quoting is possible. Purchasing is not possible. The entire functionality will be available again from May 5th 2025, 00:01 CEST. Thanks for your understanding.

iQue® 21 CFR Part 11 Software Module

Tech Support Documents Submit Review
iQue® 21 CFR Part 11 Software Module
 

Top Features of iQue® 21 CFR Part 11 Software Module 

  • Audit Trail, Electronic Records and Electronic Signature Features to Support 21 CFR Part 11 Workflows
  • Custom standardized acceptance criteria for organizational consistency
  • Operator only user role   

Popular Applications for iQue® 21 CFR Part 11 Software Module 

  • Data traceability and accountability
  • Providing detailed record keeping submissions to agencies such as FDA, EMA
  • Tracking experiment design through to quality control
System License
Item No.: 
60035
Availability: 
*Custom/bulk order quotes are provided within 24 hours of request.
iQue® 21 CFR Part 11 Software Module
iQue® 21 CFR Part 11 Software Module

Top Features of iQue® 21 CFR Part 11 Software Module 

  • Audit Trail, Electronic Records and Electronic Signature Features to Support 21 CFR Part 11 Workflows
  • Custom standardized acceptance criteria for organizational consistency
  • Operator only user role   

Popular Applications for iQue® 21 CFR Part 11 Software Module 

  • Data traceability and accountability
  • Providing detailed record keeping submissions to agencies such as FDA, EMA
  • Tracking experiment design through to quality control
Item No.:
60035
Availability:

Overview

Specifications

Choose your iQue® Software

See more products

Secure Valuable and Important Data Derived from Precious Samples 

The 21 CFR Part 11 software module for iQue® lets you replace monotonous manual record keeping with an intuitive and secure electronic record keeping system.

Designed With Regulated Environments in Mind

Specifically designed to meet the increasing requirements for regulated laboratories. Secure user roles to ensure everyone has the appropriate level of access. Electronic record keeping of all user activities from experiment design through to QC, through data analysis are included. Control the level of electronic signature frequency. Create standardized log comments for organizational consistency and ease of use. Customized audit reports can display all records or be filtered by time frames, users or experiments.

Features

  • Device/Instrument Compatibility
    iQue®

Product Information

  • Brand
    iQue®
  • System License
    1
  • User License
    1

Share Your Thoughts!

Help us amplify the customer experience by providing a review of your recently purchased Sartorius product.