Category: QC

The Quality Control (QC) category covers the testing and analytical activities that confirm the quality of raw materials, intermediates, and finished products before release. QC is one of the key pillars of GMP, ensuring products consistently meet defined specifications.

Topics include method validation and verification, stability studies, impurity profiling, chromatography, sampling, calibration, and laboratory data integrity, with a focus on practical execution and inspection-ready documentation.

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IQ, OQ and PQ: Importance in GMP

IQ, OQ and PQ: Importance in GMP

Discover the importance of IQ, OQ, and PQ in GMP, ensuring equipment and systems are installed and function correctly to...
Calibration, handling and maintenance of pH meters

Calibration, Handling and Maintenance of pH Meters

Discover essential tips for calibration, handling, and maintenance of pH meters in QC labs....
Calibration and Performance Checks of Analytical Balances

Calibration of Analytical Balances and Performance Checks

Ensure precision in QC labs with proper calibration and performance checks of analytical balances. Learn best practices for reliable and...
The role of Batch Manufacturing Records - BMR in GMP

The Role of Batch Manufacturing Records (BMR) in GMP

Learn more about Batch Manufacturing Records (BMR), essential for consistent, safe pharmaceutical production and compliance with regulatory standards....

Data Integrity in Chromatographic Peak Integration

An essential guide to maintaining data integrity in chromatographic peak integration for QC laboratories....
Worst Case Selection in Cleaning Validation

Worst Case Selection in Cleaning Validation

Optimize cleaning validation in pharmaceutical manufacturing with key strategies for selecting worst-case scenarios, ensuring product safety and efficacy....
2024 Cannabis Flower Ph.Eur Monograph

2024 Cannabis Flower Ph.Eur Monograph: A Walkthrough

Explore the new 2024 Cannabis Flower Ph.Eur Monograph, setting new quality standards for medicinal cannabis from July 1, 2024....
Person Performing Process Validation Lifecycle

Process Validation Lifecycle: Risk-Based Approach

Discover the essentials of Process Validation Lifecycle with a risk-based approach. Learn how to ensure product integrity from development to...
Gas Chromatography for testing residual solvents in GMP

Residual Solvents in GMP: Classes, Guidelines and Testing

Explore the classes and regulatory guidelines used in Residual Solvents testing in GMP....

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