Przemysl Chemiczny, Vol.86, No.8, 747-750, 2007
Validation of HPLC method used for control of cleaning procedure during the pharmaceutical substance manufacturing
The high-performance liq. chromatog. used for detn. of residual active substances during cleaning apps. for pharmaceutical prodn. was optimized and validated. The specific nature, measurement precision, linearity, detactability range and limits, accuracy and stability of solns. were taken into consideration. All quality requirements were met for prodn. of acyclovir, N-acetyltyrosine and sulfadimetoxine.