Accreditation

ABS is a pharmaceutical packaging contract manufacturer and is licensed by the TGA for production of medicinal products ranging from complementary medicines to prescription medication of some major brands.

TGA is the Australian Federal Health Department that regulates the therapeutic industry and administers standards and regulations relating to the control of ingredients, the safety and efficacy of medicines and registration of medicines in Australia. For consumer security, the TGA issue licences and also conducts on site inspections of manufacturing and packaging facilities, systems and procedures involved in the manufacture and packaging of medicinal products.

The regulations are facilitated through the code of Good Manufacturing Practice (cGMP) which outline the minimal requirements to produce therapeutic product for sale. The code of GMP covers aspects of making a product such as facilities, services, materials, people, training, clothing, hygiene, equipment and quality control. TGA routinely audits all licensed manufacturers for compliance.

ABS also hold a current APVMA license which is the federal body which administers agricultural pesticides and veterinary medicines. Like the TGA they operate to the code of GMP and have associated regulations. APVMA may audit directly or through TGA for compliance of manufacturers. ABS is licenced to package and repackage veterinary products.

Therapeutic Goods Administration Licenses

Certificate of GMP Compliance

  Licence to Manufacture and Schedule of Conditions Applicable