Some of Bova Compounding’s QUALITY ASSURANCE procedures include:

• Daily temperature and humidity monitoring and documentation
• Daily refrigerator monitoring and documentation
• Daily calibration of analytical balances
• Chemical weight verified by computer and pharmacist
• Calibration of pH meter before each use on every compounded product
• Ongoing training, testing and evaluation of aseptic personnel
• Daily random sterility and pyrogen testing of products
• Random endotoxin testing of product by independent laboratory
• Scheduled certification of sterile environment
• Independent lab testing of air and surface samples for the cleanrooms
• Cleanrooms tested by NATA certified personnel, exceeding guidelines with a class 6 cleanroom
• Continuous cleaning of compounding environments
• Compounding software with backup for continuous record keeping:
  • Formula
  • Procedure/technique
  • Lot numbers
  • Prescription numbers
  • Expiration dates
• Chemicals obtained from TGA suppliers where possible
• Regulated storage of raw materials and end products
• Personnel trained and certified in procedures for each type of aseptic event
• Personnel dedicated to policies and procedures to ensure a quality product.

Bova Compounding follows strict guidelines when preparing sterile and Cytotoxic products. We have state of the art negative pressured room for all our Cytotoxic products as well as a positive pressured room for all our sterile medication.

Download our Adverse Reaction document