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
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