Category: Quality Control
This article describes about elemental impurities, Its classification and possibilities from where it can be generated. Elemental Impurities for Pharmaceutical Drug Products What is mean by Elemental Impurities ? Elemental impurities are trace amounts...
What is mean by Chromatography? Chromatography is a Technique used to separate and analyze the components of a mixture. It involves passing a mixture through a stationary phase i.e. column, which may be a...
This article provided Comprehensive information on Force degradation Study (FDS), Methodology of testing, Why it is required in pharmaceutical industry. Force Degradation Study (FDS) – A Comprehensive Guide What is mean by Force Degradation...
This article contains about Analytical method validation process, parameters, Advantages and prerequisites. Analytical Method Validation- A Comprehensive Guide What is mean by Analytical Method Validation? Analytical method validation is a type of validation which...
This article describes about Comprehensive information on Gas Chromatography. Comprehensive information on Gas Chromatography (GC) What is mean by Gas Chromatography and It’s Principle? Gas chromatography is a technique used in analytical chemistry to...
This article describes about Comphrensive information on HPLC (High Performance Liquid Chromatography) technique. What is mean by HPLC and it’s Principle ? HPLC stands for High Performance Liquid Chromatography, is a technique used to...