Abstract

Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm!

Author(s): Odegard Russell D

Issue: Mar/Apr 2008 - Compounding Around the World

Page(s): 130-135

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  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 1
  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 2
  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 3
  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 4
  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 5
  • Quality-Control Analytical Methods: Minimizing the Probability of Out-of-Specification Preparations: Results that Make You Say…Hmmm! Page 6

Abstract

To prevent compounding of an out-of-specification preparation, the possible causes of such an error must be identified and eliminated. Implementation of simple practices can decrease the probability of errors, resulting in a safer situation for both the patient and the pharmacy. The United States Pharmacopeia–National Formulary is the standard-setting reference for compounding procedures; all compounding pharmacists should read and adhere to those standards. This article discusses these standards as they relate to drug potency, sterility, endotoxin, and particulate matter results.

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