This course provides a comprehensive coverage of the method development and validation requirements that are essential to progress a pharmaceutical compound, at each stage of product development.

The authors discuss the theory of ion mobility spectrometry, its benefit over HPLC analysis in cleaning verification, and the experimental considerations for method validation and validation.

In this interview, Michael Dong discusses stability-indicating methods such as UHPLC, in pharmaceutical analysis. At Pittcon, Michael will introduce a 3-pronged template approach to HPLC method ...

Thermo Fisher Scientific and ChromSword have collaborated to launch an automated high performance liquid chromatography (HPLC) and ultra-high performance liquid chromatography (UHPLC) method ...

The authors describe a method-validation-by-design (MVbD) approach to validate a method over a range of formulations using both design-of-experiment and quality-by-design principles to define a design ...

Many people use high performance liquid chromatography, yet very few understand how they work. HPLC seems like a complicated combination of motors, gears, pressures, flows, chemistry, physics and ...

High performance liquid chromatography (HPLC) is a technique in analytical chemistry used to separate, identify, and quantify each component in a liquid mixture. The Agilent 1260 Infinity Quaternary ...

A study published in Current Pharmaceutical Analysis presents a validated RP-HPLC method for analyzing orlistat, an anti-obesity drug. The method ensures accurate quantification and is aligned with ...

This course provides a comprehensive coverage of the method development and validation requirements that are essential to progress a pharmaceutical compound, at each stage of product development.