This course is designed to demonstrate how to properly perform a filter integrity test on a sterilizing filter for compounded sterile preparations.

This course discusses the items appropriate items that should be in a hazardous spill kit as well as demonstrates the proper way to clean and dispose of hazardous chemical.

This course demonstrates how to use the QI Medical Chemo Test to assess the technique of operators while compounding with hazardous chemical.

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The Competency Testing in Aseptic Manipulation video series provides pharmacy professionals with essential training to achieve and maintain competency in sterile compounding. Covering cleanroom entry, garbing, hand hygiene, sterile glove donning, gloved fingertip sampling, media fills, and surface sampling, the series delivers practical demonstrations aligned with USP requirements. Learners gain the confidence, knowledge, and skills needed to pass competency testing and ensure safe, contamination-free compounding.

This lesson provides a comprehensive overview of environmental monitoring (EM) in cleanroom environments. Learn the purpose and types of EM—viable and non-viable—along with proper sampling techniques, incubation practices, data interpretation, and trend analysis. The training emphasizes regulatory compliance, contamination control, and the critical role of EM in ensuring patient safety and product quality in sterile compounding.

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This lesson provides a comprehensive overview of environmental monitoring (EM) in cleanroom environments. Learn the purpose and types of EM—viable and non-viable—along with proper sampling techniques, incubation practices, data interpretation, and trend analysis. The training emphasizes regulatory compliance, contamination control, and the critical role of EM in ensuring patient safety and product quality in sterile compounding.

This course provide infomation on how to properly perform surface sampling and the current standards for incubating samples

About the Course This course will provide the learner with the knowledge to about the design of cleanroom facilities and the engineering controls used

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Master the correct technique for glove fingertip and thumb sampling to meet USP compliance requirements. This lesson guides you through the purpose, procedure, and documentation of fingertip sampling during media fill and personnel qualification. Learn how to collect samples aseptically, interpret results, and support ongoing assurance of sterile compounding competency.

This course is intended to explain the purpose of a media fill and how it must be done according to USP Chapter .

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Gain the skills to accurately interpret microbial growth on environmental monitoring media and respond effectively to action limit excursions. This lesson covers identifying colony-forming units (CFUs), comparing results to ISO classification limits, documenting findings, and initiating appropriate corrective and preventive actions (CAPAs). Designed to support USP , , and FDA cGMP compliance in cleanroom environments.

This lesson provides comprehensive training on performing a media fill simulation test—an essential qualification for personnel involved in sterile compounding. Learn how to prepare growth media, simulate aseptic compounding procedures, incubate and inspect units, and document results. The training supports USP and FDA cGMP compliance to ensure aseptic technique competency and protect patient safety.

Learn how to properly perform surface sampling in cleanroom environments to support environmental monitoring and contamination control. This lesson covers the selection and use of contact plates and swabs, proper sampling technique, labeling, incubation, and documentation. Emphasis is placed on USP , , and FDA cGMP compliance to ensure sterile compounding quality and patient safety.

Learn how to properly perform the Gel-Clot Limulus Amebocyte Lysate (LAL) endotoxin test—a critical method for detecting bacterial endotoxins in sterile pharmaceutical products. This lesson covers reagent preparation, sample handling, incubation procedures, and result interpretation, with emphasis on avoiding inhibition or enhancement. Aligned with USP and FDA guidance, the training ensures accurate endotoxin detection and compliance in sterile compounding.

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