We operate a NATA approved sterile compounding laboratory that was built in 2018 to the new U.S. PHARMACOPEIA <797> & PHARMACY BOARD OF AUSTRALIA REQUIREMENTS.
Our ISO 5 Environment with an ISO 3 hood keeps our compounding laboratory highly sterile. We assure our clients with high product standard and quality with our ongoing and daily environmental monitoring.
Our in-house quality assurance procedures and processes include:
- environmental monitoring,
- sterility testing,
- endotoxin testing,
- batch testing,
- 24-hour temperature control,
- 24-hour humidity monitoring,
- 24-hour pressure monitoring
We strive to ensure confidence in the products we produce, and ensure they are of the highest quality. As such, we purchase raw materials from TGA (Therapeutics Goods Administration) approved suppliers.
Our high qualified and trained staff in sterile compounding have experience with training in government department and private sterile hospital, along with continual internal and external accredited training.
Your enquiries are welcomed and we will work with multiple healthcare practitioners, medical clinics, and patients to ensure your demands are met. Please refer to the contact us page for any enquiries.