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Determination of the Working Range of the Laboratory Balance in Accordance to USP Chapter 41
26 Oct 2016This white paper describes how to determine the working range of a laboratory balance in accordance to Chapter 41 of the USP (United States Pharmacopeia) regulatory document. The white paper defines what is meant by the term ‘minimum initial weight’ and describes the requirements of the new Chapter 41. It also explains how the software application Q-App USP V2.0 can support the user of the Cubis® range in fulfilling the requirements of Chapter 41.
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Balances and Moisture AnalyzersBalances & Moisture Analyzers / weighing scales measure static or dynamic loads. Features to consider when choosing an analytical balance include accuracy, capacity and resolution. Additional features and specialized balances include enclosures for weighing powder, microbalances for measuring small quantities, portable balances, moisture analyzers, top loading balances and internal calibration for measurements over time or with varied temperature.Drug DosageDosage is the size or frequency of the administration of a drug. Determination of the dosage of a drug is critical in pharmaceutical development to ensure the optimum balance between efficacy and toxicity.Software SolutionPharmaceuticalsPharmaceuticals are medicinal drugs used in healthcare to diagnose, prevent, cure and treat illnesses. Pharmaceuticals that are excreted after use appear in wastewater and can have detrimental effects on the environment.Drug DevelopmentDrug development refers to the process of bringing a new drug to market.