The author describes strategies for analytical method development that are helpful in achieving quality by design and efficiency. Get the essential updates shaping the future of pharma manufacturing ...

SFC Europe 2025—the 19th International Conference on Packed Column Supercritical Fluid Chromatography and Related ...

The attributes of the DS or DP that are to be tested to obtain the necessary information about product quality safety and efficacy are determined during the Drug Development stage. The information ...

When transferring a method from R&D to quality control, success hinges on discovering where “the best” and “the most reliable” intersect. MINERVA STUDIO - STOCK.ADOBE.COM Analytical method transfer ...

Analytical methods must be validated to provide reliable data for regulatory submissions. These methods are essential for a number of purposes, including testing for QC release, testing of stability ...

DS InPharmatics Head of Analytical Services, Colman Byrne joins the show to share his experience in analytical method development and validation. Colman is the most senior analytical services expert ...

This field has evolved considerably through the integration of systematic design strategies, notably the incorporation of Analytical Quality by Design (AQbD) principles and robust statistical tools ...

Each department, from production to clinical research, deals with three types of work: maintenance, routine, and project work. The work shares vary with the nature of the work, but all departments ...

The RGB model, which combines red (analytical performance), green (environmental impact), and blue (practicality), is at the heart of the concept of white analytical chemistry (WAC). While this ...