000 a
999 _c20253
_d20253
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005 20231207095201.0
008 231207b xxu||||| |||| 00| 0 eng d
040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _922309
_aRajmane, Akash D.
245 _aReview of HPLC method development and validation as per ICH guidelines
250 _aVol.13(2), Apr-Jun
260 _aRaipur
_bAsian Pharma Press
_c2023
300 _a143-151p.
520 _aMethod development and validation are continuous processes that progress in parallel with the evolution of drug products. Changes encountered during drug development may require modifications to existing analytical methods. These modifications to the methods, in turn, may require additional validation. The advent of new techniques and improved instrumentation in the field of analysis may give way to more sensitive, precise, and accurate methods if the existing methods are erratic or unreliable; time-consuming, or too expensive. Thus, continuous new analytical method development and validation activities are essential for the growing drug development programs.
650 0 _94639
_aPHARMACEUTICS
700 _922308
_aShinde, Komal P.
773 0 _dRaipur A & V Publications
_x2231-5667
_tAsian journal of pharmaceutical analysis
856 _uhttps://ajpaonline.com/AbstractView.aspx?PID=2023-13-2-13
_yClick here
942 _2ddc
_cAR