Brookfield Medical Surgical Supply Inc. compounds preservative free steroid injections for pain centers, doctor’s offices, surgery centers and hospitals. These products consist of Triamcinolone Acetonide, Methylprednisolone Acetate and Betamethasone Sodium Phosphate. Our facility is an FDA registered, 503B outsourcing facility, therefore, we follow the current Good Manufacturing Practices (cGMP). This higher standard of regulations and practices generate quality products you can depend on. All of our products are rigorously tested prior to being released. Sterility, potency and endotoxin tests are performed on every batch of compounded products. Samples from each batch are submitted to an FDA registered Lab where these tests are performed. All test results are reviewed upon receipt by our Quality Control Officer. Once approved, the batch of CSP may then be dispensed. The certificate containing the test results for any given batch are available upon request.
Our sterilization methods consist of filtration and terminal sterilization. Quality control measures are used to verify the effectiveness of the sterilization method. These quality control measures include the use of biological indicators, Sterigage Chemical integrator strip (type 5) and filter integrity testing.
Our formulas are controlled and verified prior to compounding. All ingredients are purchased from FDA Registered manufacturers. All ingredients sent to the facility come with a Certificate of Analysis which is reviewed and approved prior to use. Each ingredient is barcode scanned during the compounding process for verification. Each formula is then verified by a second pharmacist for quality control. After all components of the compounding record has been checked by the secondary pharmacist, each individual vial will then be visually inspected. We perform a 100% visual inspection of the product under magnification prior to distribution.