Tag: QC

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Featured image showing laboratory documentation and the title “5 Key Differences Between OOS, OOT, and OOE Results.”

5 Key Differences Between OOS, OOT and OOE Results

Learn the key differences between OOS, OOT, and OOE results, how each directs investigation depth, CAPA actions, and regulatory response...
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....
People performing Process Validation in GMP facility

Process Validation in GMP

Discover the essentials of Process Validation in GMP, ensuring pharmaceutical quality through scientific and regulatory practices....
Out of Specification Results Dealing with OOS Investigations in Pharma

Out of Specification Results: OOS Investigations in Pharma

Learn about all the phases of addressing Out of Specification (OOS) results in the pharmaceutical industry...
Cleaning Validation of Equipment in Pharmaceutical Industry

Cleaning Validation In the Pharmaceutical Industry

Explore the essentials of cleaning validation in the pharmaceutical industry, including all necessary steps, challenges, and regulatory standards....
Quality Assurance vs Quality Control in GMP

Quality Assurance vs. Quality Control in GMP: Key differences

Explore the critical differences between Quality Assurance and Quality Control in GMP and learn more about their role within the...

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