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Overview of pharmaceutical quality control steps and implementations

GMPSOP

This article will focus on some of the common activities performed in quality control facilities daily to maintain the expected level of compliance and ensuring product quality. This means that the analytical methods consistently generate true results with precision and accuracy every time. accuracy, precision, etc.)

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Ethical Nutraceuticals: Need of the hour

Express Pharma

This article is a summation of the inferences drawn and lessons learnt from the views, concerns and insights shared by experts on this knowledge-sharing platform. They also examined how technology can be leveraged and effectively deployed to provide specific dosages and ingredients as per patients’ varying needs.

Dosage 101
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Stability testing overview for Pharmaceutical products

GMPSOP

This article will explore different types of stability studies, designing of stability trial testing program, aspects of stability protocol, different storage conditions, determination of shelf life by analysing stability trial results and common problems that can invalidate a stability testing.

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Importance of acceptance criteria in analytical method transfer

GMPSOP

Rather, it is a supplement to the validation study that demonstrates the analytical method’s reproducibility, or inter-laboratory precision. In the later part of the article, we will explain how to determine testing patterns and acceptance criteria for analytical method transfer exercises sometimes abbreviated as AMTE.

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What are the elements of quality control process in pharmaceuticals

GMPSOP

Validated test method A test method comprehensively describes all procedures used in sample analysis. Analytical test method validation guarantees that your test method is robust enough to provide evidence if your product meets the predetermined product specification or conforms to the failure of a product.