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Centers

Our state of the art compounding facilities are designed to provide high-quality preparations following USP guidelines for sterile compounding.  The key to providing a safe admixture resides in using the principles of aseptic processing to maintain sterility of the FDA approved components throughout the compounding process.  We have surpassed the minimum guidelines for clean room design, operation and maintenance to take the art of compounding to a new level.  From the use of minimum ISO 6/Class 1,000 and ISO 7/Class 10,000 clean rooms to our meticulous attention to the detail of environmental monitoring and sanitization, we utilize a process for compounding sterile preparations that exceeds all appropriate guidelines and regulations.

• Monitoring
  Environment controls include the practice of routine monitoring of the facility and clean room environment for temperature, air quality and sterility
  
  
• Routine Sanitization
  Adherence to a strict routine for the sanitization of the ISO 5/Class 100 Laminar Air Flow Workbench (LAFW) clean room compounding fixtures, floors, walls, ceiling and equipment ensures sterility is maintained at every step of the process.
  
  
• Design
  Facility design creates a unique environment able to ensure the correct flow for compounding sterile admixtures that significantly reducesthe potential for contamination or process error.

 

 

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