Autopak-Vetla b maintain their record for the manufacture of both branded and generic formulations by applying a number of industry-standard benchmarks. These include:
- ISO9002 accreditation
- cGMP systems
- The VETLAB division holds a TGA (pharmaceuticals) licence for manufacturing hospital grade disinfectants and has been audited for compliance to EN46002
- QA standards that conform to the National Registration Authority for Agricultural & Veterinary Chemicals
- The factories are fully licensed, meeting the stringent Environmental Protection Authority and WorkCover Authority requirements
- Overseas auditors located in the USA and Europe from the multinational companies served regularly audit the facilities
- A documented process of using specifications, control methods and batch records is followed under cGMP. Regular testing is carried out on raw materials, bulk mixes and finished products
- The quality control laboratory is equipped with a wide range of instruments capable of most chemical testing including chromatography, spectrometry and conventional wet methods