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 ...

As analytical technology continues to advance, both regulatory agencies and pharmaceutical companies are keen to avail themselves of these enhancements. In the case of chromatography, evolution from ...

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 ...

Course Topics Include: – FDA, ICH and USP Validation Requirements – Applying Validation Studies Consistent with Method Purpose – GMP Compliance during Validation – Validation Acceptance Criteria – ...

This course is a classroom-based course covering all the practical theory about liquid chromatography and its related techniques including liquid chromatography-mass spectrometry. This course is ...