SandsRx is now offering sterile compounded prescriptions from our USP 797 and USP 800 compliant compounding labs. Each of our sterile compounds are prepared in ISO certified clean rooms at our headquarters facility in Wylie, Texas.
Sterile compounding involves preparing a medication in an environment free from bacteria, viruses, or any other potentially infectious microorganisms. According to the United State Pharmacopeia, Sterile compounding is further defined to include any manipulation of sterile or non-sterile product intended to produce a sterile final product. This type of compounding is used for medications that will be administered either IM, IV injections, or directly into the eyes.
Testing and Quality Assurance Program:
We are committed to ensuring that compounded sterile products are safe, effective and meet the highest quality standards. We use a combination of peer reviewed literature and our own stability studies to support the integrity of our products. Our quality control and quality assurance programs include product verification, routine testing, in-process controls, and a rigorous inspection process by our specialized sterile compounding team.
Sterile Compounding Dosage Forms:
- Injections (aqueous and oil vehicles)
- IV admixtures
- Ophthalmic (solutions, suspensions, sprays, and ointments)
- Irrigating Solutions
- Inhalation solutions (multiple ingredients can be combined to improve compliance)
SandsRx is proud to have achieved both the PCAB and NABP’s compounding accreditations. We are committed to operational excellence, patient safety, and quality of care. Achieving the PCAB and NABP accreditations are a testament to our dedication to the safety and well-being of our patients.