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 ...

Testa Analytical highlights how its FlowChrom real-time flow monitoring system makes it possible to directly compare and ...

TESTA Analytical reports how its FlowChrom real-time flow monitoring system enables direct comparison and transferability of HPLC Methods and results between instruments in different locations. It is ...

Learn how to approach method speed up, optimization and transfer when modernizing pharmacopeial monograph methods. This webcast will discuss the use of superficially porous particle (SPP) columns on ...

In the pharmaceutical industries, validation of analytical methods is a critical process that confirms the reliability and appropriateness of a method for its intended application. Method validation ...

With the USP formally implementing a series of test method updates to USP 661.1 and USP 661.2 effective December 1 st 2025 it is imperative that the CS Analytical Team be prepared to help our client ...