Why Choose Us
We have testing facilities located both in Sydney and in Brisbane. Our state-of-the-art facilities were purpose-built for efficient sample processing, for a compliant testing environment and to allow for future expansion and diversification. The cleanroom setup in our Sydney site allows sterile products testing to be done according to the respective standards.
OUR COMMITMENT TO QUALITY
Our commitment to quality in our testing and consulting services is one key distinction that sets us apart from others.
Our Quality System is based on PIC/S Guide to Good Manufacturing Practices for Medicinal Products, PE 009-8 and International Organization for Standardization (ISO) 17025. We are assessed by the Therapeutic Goods Administration (TGA), the Australian Pesticides and Veterinary Medicines Authority (APVMA), the United States Food and Drug Administration (US FDA), the National Association of Testing Authorities (NATA) and the Office of the Gene Technology Regulator (OGTR). You can download copies of our licenses and accreditations from our ams Literature Library here.
In line with our dedication to quality, we place great importance in staff training and development as they are key assets in our business.
MEETING AGREED TURNAROUND TIME (TAT)
To meet TAT goals, all aspects of the laboratory testing process must be considered, ie, everything from order entry to results reporting. At Eurofins | ams, we take pride in being able to meet the TAT agreed with our customers without compromising quality. We are able to do so with efficient planning, proper training and optimization of workflow.
PROVIDING ACCESS TO EUROFINS' GLOBAL NETWORK OF BIOPHARMA SERVICES
Eurofins is a first-class Contract Research Organization (CRO), working with pharmaceutical, chemical, biotechnology, medical device and cosmetic clients. The Group covers the whole chain of drug development thanks to an international network of laboratories and testing units with global reach, uniform QA systems and high quality services.