Category: Method Validation

Detection Limit (DL) and Quantification Limit (QL) In Method Validation

Detection Limit (DL) and Quantification Limit (QL) In Method Validation

Detection Limit (DL) and Quantification Limit (QL) In Method Validation Introduction and outcome Detection Limit and Quantification Limit are the...

How to perform Specificity in Analytical Method Validation

How to perform Specificity in Analytical Method Validation

How to perform Specificity in Analytical Method Validation Introductions and Outcome Specificity is one of the important parameters of Analytical...

How to Perform Accuracy in Analytical Method Validation

How to Perform Accuracy in Analytical Method Validation

How to Perform Accuracy in Analytical Method Validation Introduction and outcome Accuracy is one of the important parameters of the...

Validation and Verification: How and Where to Apply

Validation and Verification: How and Where to Apply

Validation and Verification play a crucial role in pharmaceutical analysis.It is impossible for any Pharmaceutical company to perform the Analytical method validation of all the methods due to various reasons like timeline, cost and resources. That is why companies also do the Analytical Method Verification or mini-validation in some cases. Since there are no guidelines on the Analytical method verification/mini-validation and hence there is a lot of confusion among Pharma professionals related to the same. In this article, you will learn skill-based knowledge on method validation and verification, difference between validation and verification, applications, advantages with case studies and FAQs.

Analytical Method Transfer or Technology Transfer: The Best Practices

Analytical Method Transfer or Technology Transfer: The Best Practices

This article describes analytical method transfer or technology transfer or tech transfer procedures, and protocol and with FAQs

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