Data Integrity in Pharmaceutical Quality Control Infographic | Sartorius

Infographic: Data Integrity in Pharmaceutical Quality Control

In partnership with American Pharmaceutical Review

Last updated: September 2023

Overview

Large amounts of data are generated during pharmaceutical research and development, clinical trials, and manufacturing processes. It is critical that pharmaceutical companies take steps to ensure data integrity at every stage of the drug development process.

This infographic provides an overview of key terms and definitions, points of compliance, and ways to achieve quality control and data integrity.


  • Document type: Infographic
  • Page count: 1
  • Read time: 3 minutes


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Key Takeaways

  • Understand the ALCOA principles and their application

  • Navigate GAMP guidelines and 21 CFR Part 11 compliance

  • Understand important terms and definitions

  • Discover Sartorius Ingenix Suite of software for optimal data management

This Resource is Designed for:

  • People Working in QC Labs
  • QC Manager
  • Compliance Officers
  • Lab Technicians in the Pharmaceutical Industry

Applications Supported:

  • Pharmaceutical Quality Control (QC)
  • Data Management Systems
  • Data Audit Trails
  • Data Integrity
  • ALCOA
  • GAMP
  • Validation Documentation
  • 21 CFR Part 11

Please Complete the Form to Access the Infographic