I have always written out in the analytical method to "prepare two primary standards that are 120% of the normal concentration of target analyte by weight (in duplicate, two separate weighings required); then serially dilute the primary to make a "100% level", then dilute the primary to obtain an "80% of normal level" for the active ingredient (analyte). This yields three calibration points representing 120%, 100%, and 80% normal of the analyte concentration; assay these standards and contruct a regression line; acceptance criterion is R-square greater than or equal to 0.95 (which means that greater than or equal to 95% of the variance in the peak area response is explained differences in analyte concentration--with the rest being written off as random error); then perform the same serial dilution of the duplicate preparation, inject them as "unknowns", and quantify them against the cal curve; the resultant values for the unknowns should be between 95% to 105% of the true value".
Hope this helps.
Jumpshooter