Author(s): N. Chittemma and M. Manimala
ABSTRACT The aim of the study was to develop and validate RP-HPLC method for the analysis of cisbromobenzoate in marketed tablets and pure form.The methods was validated in terms of system sutiability,linearity, accuracy (%Recovery), precision (system precision& intermediate precision), speficity,ruggedness ,and robustness. The method found to be linear (R2 =0.999) and accurate. The methods was also found precise (% RSD< 2%) and robust. All validation parameters were within the acceptable range as per International Conference on Harmonization (ICH). Parameters of validation prove the precision of the method and its applicability for the determination of cisbromobenzoate in pharmaceutical tablet formulations.