You may require this code if you are involved in the manufacture of biologicals and therapeutic goods.
The standards and principles contained in this Code are intended to serve as a reference for practice, as requested under the Pharmaceutical Inspection Convention or the Pharmaceutical Inspection Co-operation Scheme. It covers areas such as compliance, quality management, personnel, premises and equipment, and documentation. Please note that there are various codes for medicines, medical devices and chemicals which are amended on a regular basis.
Please consult the Contact Officer for more information and to ascertain the level of compliance (if any) that may be required by your business