The weighing of a sample is typically the first step in an analytical procedure, and therefore has the potential to propagate through the process and cause the inaccuracy of the final result. On 1 st December 2013, the new regulations of USP Chapter 41 went into effect and this chapter is mandatory in a Pharmaceutical Quality Control (QC) laboratory, where weighing is a fundamental step in almost every workflow. What is The USP Chapter 41 (USP41)?Ĭhapter 41 of the USP standards is titled ‘balances’ and refers to the mandatory requirements for the accurate weighing of materials using a balance. You can find out more about The USP on their website. The Food and Drug Administration (FDA) are responsible for their enforcement. The USP drug standards are used in over 140 countries and include identity, strength, quality and purity of substances manufactured. The United States Pharmacopeia (USP) is a scientific organisation responsible for setting the official public standards for drugs and drug products in the USA. USP Chapter 41 (USP41) Weighing Requirements for Balances What is the USP?
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