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...Pharmacy risk assessment for mass measurement processes content introduction errors gross error systematic random balance accuracy and precision in pharmaceutical industry balances used requirements according to quality control examination verify or calibrate estimation criteria managing reference measurements analysis practical matters resolution electronic sensitivity change standard procedure changes testing non linearity test differential with the use of tare sop example summary eccentricity centricity leveling repeatability calculation practice how often should parameters be tested low all purpose uncertainty masses rule minimal instance permissible a routine measuring instrument life cycle weighing systems validation external factors process oscillations vibrations breeze air temperature during electrostatics sample structure hygroscopicity magnetism as interfering factor functional abilities automatics contemporary create wrong impression that they offer guaranteed such attitude...