Xpharm Series Software |link| Direct

Xpharm was often validated for compliance (electronic records and signatures), making it suitable for GLP (Good Laboratory Practice) and GCP (Good Clinical Practice) environments. Audit trails tracked every modification to the dataset or analysis parameters.

Power users could create script files (often .BAT or custom macro languages) to analyze hundreds of studies overnight, a feature not common in early graphical competitors. xpharm series software

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| Parameter | Meaning | Typical use | |-----------|---------|--------------| | AUC(0-t) | Total exposure from time 0 to last measurable conc. | Compare total drug absorption | | AUC(0-inf) | Extrapolated total exposure | IV bioavailability | | Cmax | Peak concentration | Safety/efficacy peak | | t½ | Elimination half-life | Dosing interval design | | CL/F | Apparent clearance | Dose adjustment | "suggestion":"pharmaceutical LIMS comparison"