Logo - International Journal of Pharmaceutical Compounding

Quality-Control Analytical Methods: Designing a Quality-Control Potency Testing Program for a Compounding Pharmacy

Author(s):  Zolner William J

Issue:  Sep/Oct 2009 - Veterinary Compounding
View All Articles in Issue

Abstract:  Undeniably, one of the most important considerations in a compounding pharmacy’s procedures is quality. Developing a comprehensive quality-control potency program must begin with the most basic activities performed at a compounding pharmacy to the most crucial activities. If the basics are not met, the crucial activities of compounding sterile and non-sterile preparations and the quality of the end product are in jeopardy. Basic definitions are provided in this article as well as a discussion on a three-step method on setting up a quality-control potency testing program, to include (1) process design and how to reduce the potential of variations and mistakes in compounded preparations, (2) process verification, and (3) how to set up a sampling plan to monitor ongoing quality. Also included are suggestions on how to get started on the development of a quality-control potency testing program.

Related Keywords: William J. Zolner, PhD, quality control, quality assurance, potency testing, compounding mistakes, process design, sampling plan

Related Categories: QUALITY CONTROL

Purchase this article for download in electronic PDF format from IJPC at for $35 at:
http://www.ijpc.com/Products/ProductAddToCart.cfm?PID=3009

Search the entire IJPC archive by keyword, topic, or issue at:
http://ijpc.com/Products