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 ...

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 ...

Biotech Fluidics has launched a new flowmeter kit that provides fast, precise, and reliable validation of the ongoing performance of any HPLC pump. All HPLC separations are reliant on a stable flow of ...

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

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 ...

Research peptide reference standards in the Koi Peptides laboratory catalog have broadened with the addition of new reference compounds for in vitro analytical use.