Compounding Quality Center of Excellence updates
Compounding Quality Center of Excellence

Improve your aseptic processing techniques  

Register for our instructor-led training courses in Raleigh, N.C.: 

  • Environmental Monitoring, July 14-16, 2026: Monitoring the sterile drug production environments is critical for detecting and controlling microbial contamination. Learn sample collection methods and contamination control practices to comply with federal regulations and ensure drug quality and patient safety. 
  • Cleanroom Design and Operation, July 21-23, 2026: Drugs intended to be sterile must be free of impurities and contaminants. Enhance your understanding of cleanroom design, operation and maintenance for sterile drug production.  
  • Sterile Drug Compounding, August 11-13, 2026: Aseptic technique is critical in sterile drug compounding. Learn the fundamentals of sterile drug production by integrating aseptic processing, sterile filtration, cleanroom operations, facility cleaning and disinfection, aseptic process simulation (media fills) and environmental monitoring. 

Opportunities to prepare for these training courses 

Prepare for these in-person trainings with our self-guided online training courses – Aseptic Process Simulations (Media Fills), Airflow and Insanitary Conditions and Sterility Assurance – and webinars – Cleanrooms and Cleanroom Behaviors: Why they Matter and Environmental Monitoring in Compounding.  

These training courses and others are in collaboration with the Parenteral Drug Association (PDA).  

FDA’s Compounding Quality Center of Excellence aims to improve the quality of compounded drugs, especially those made at outsourcing facilities. We encourage outsourcing facilities and others to get involved with the Center of Excellence by taking our training courses, in-person and online, attending our annual conference and other activities. 


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