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USP Chapter 41 Weighing Requirements on Balances in Pharmceutical Quality Control
USP Chapter 41 weighing requirements are mandatory in a Pharmaceutical Quality Control laboratory, where weighing is a fundamental step.
100% traceability in compliance with GLP and accredited procedures
Reference samples, called standards, are required to determine the concentration of chemical compounds using highly sensitive quantitative analytical procedures
Improve accuracy and efficiency of your day-to-day laboratory measurement tasks
This "Essential Laboratory Skills" Guide supports lab operators to recognize and avoid potential error sources and ultimately increase laboratory efficiency.
Identification of inefficiencies and specific bottlenecks in weighing is key to optimize laboratory processes and performance.
Weighing results that are valid, reliable and correct from the start
Weighing in the safe weighing range ensures results are valid, reliable and right the first time.
The Ultimate Knowledge Tool for Weighing Champions
Preparation of buffers, standards and samples often requires weighing followed by dissolution to a defined volume or dilution in volumetric flasks
All balances undergo a monthly repeatability test in accordance with U.S. Pharmacopeia
Ensuring that a balance is level is crucial to obtaining accurate weighing results
Check the Sensitivity of Your Balances
As is the case for a number of other businesses, the pharmaceutical industry tends to have strictly regulated areas, for example in quality control procedures
Learn more about pros and cons of different levels of weighing data management, as well as tips how to optimize the integration of your weighing data
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