Preparation of sterile products must be given top priority to assure the safety and therapeutic efficacy of the extemporaneously prepared products. Everyone preparing sterile preparations should follow the USP Chapter 797 Guidelines.

Sterility can be achieved through proper employee training, compounding facility design, construction, operation, control and maintenance, good aseptic techniques and habits, process validation and verification of aseptic compounding procedures.

We follow the guidelines set forth and have a clean room to make sterile products. The quality of our clean room environment is maintained by controlling the temperature, humidity and by isolating organisms that may cause contamination. We use a filtration system or heat sterilization with a convection oven to remove contaminants.

Care is taken during the compounding process to ensure that the preparation made is of the highest quality. Large batches are sent to a certified, quality control lab for stability, sterility and potency testing.

Areas that we are currently preparing sterile products are intrathecals, inhalations ophthalmology solutions and injectables.

Please feel free to call us for more information on our clean room and aseptic procedures.