Category: Analytical Method Validation

Robustness Parameters in HPLC: pH, Flow Rate, and Temperature

Robustness Parameters in HPLC: pH, Flow Rate, and Temperature Robustness Parameters in HPLC: pH, Flow Rate, and Temperature In pharmaceutical development, validation is a critical component to ensure the precision, safety, and efficacy of products. This article provides a structured…

Ruggedness Testing Using Inter-Laboratory Variations

Ruggedness Testing Using Inter-Laboratory Variations Ruggedness Testing Using Inter-Laboratory Variations As pharmaceutical and biologics professionals, understanding the importance of robust instrument validation during analytical method development is critical to maintain compliance with regulatory guidelines. This tutorial provides a comprehensive step-by-step…

How to Perform Robustness Studies in Analytical Validation

How to Perform Robustness Studies in Analytical Validation How to Perform Robustness Studies in Analytical Validation The pharmaceutical industry is governed by strict regulations and guidelines designed to ensure the safety and efficacy of products. With the necessity for meticulous…

Method Robustness vs Ruggedness: What’s the Difference?

Method Robustness vs Ruggedness: What’s the Difference? Method Robustness vs Ruggedness: What’s the Difference? In the field of pharmaceutical validation, understanding the concepts of robustness and ruggedness is crucial for ensuring that analytical methods deliver reliable results consistently. This article…

Importance of R² in Linearity Evaluation and Common Pitfalls

Importance of R² in Linearity Evaluation and Common Pitfalls Importance of R² in Linearity Evaluation and Common Pitfalls In the pharmaceutical and biotechnology sectors, the validation of analytical methods is crucial to ensure that they meet regulatory expectations and product…

How to Document Linearity and Specificity Results for Audits

How to Document Linearity and Specificity Results for Audits How to Document Linearity and Specificity Results for Audits In the pharmaceutical industry, the validation of analytical methods is a critical component to ensure compliance with regulatory standards such as FDA,…

Troubleshooting Linearity Failures in Method Development

Troubleshooting Linearity Failures in Method Development Troubleshooting Linearity Failures in Method Development Step 1: Understanding User Requirements Specification (URS) and Risk Assessment In developing effective validation protocols, the first critical step involves creating a User Requirements Specification (URS). A well-defined…

Validation of Assay Methods: Accuracy and Precision Templates

Validation of Assay Methods: Accuracy and Precision Templates Validation of Assay Methods: Accuracy and Precision Templates Step 1: User Requirements Specification (URS) & Risk Assessment The validation lifecycle begins with the User Requirements Specification (URS), which serves as the foundation…

Matrix Effect and Specificity in HPLC and UV Methods

Matrix Effect and Specificity in HPLC and UV Methods Matrix Effect and Specificity in HPLC and UV Methods This article provides a comprehensive, step-by-step tutorial on the product validation process within the context of HPLC and UV analytical methods. The…

Precision Criteria for Stability-Indicating Methods

Precision Criteria for Stability-Indicating Methods Precision Criteria for Stability-Indicating Methods In the pharmaceutical industry, the validation of analytical methods is critical to ensuring safety and efficacy in products. The iq oq and pq validation process is fundamental in establishing the…