Acronyms used in this Manual
AAT |
Administrative Appeals Tribunal |
ACN |
Australian Company Number |
ADI |
Acceptable daily intake |
ARfD |
Acute reference dose |
ATS |
Application Tracking System |
APVMA |
Australian Pesticides and Veterinary Medicines Authority |
AQIS |
Australian Quarantine and Inspection Service |
ARBN |
Australian Registered Body Number |
CCI |
Confidential commercial information |
CSIRO |
Commonwealth Scientific and Industrial Research Organisation |
DEW |
Department of the Environment and Water Resources |
DHA |
Department of Health and Ageing |
EAGAR |
Expert Advisory Group on Antimicrobial Resistance |
EC number |
Enzyme Commission number |
EMEA |
European Medicines Agency |
FAISD Handbook |
Handbook of First Aid Instructions, Safety Directions and Warning Statements for Agricultural and Veterinary Chemicals |
FDA |
United States Food and Drug Administration |
FSANZ |
Food Standards Australia New Zealand |
GMO |
Genetically modified organism |
GMP |
Good manufacturing practice |
MORAG |
Manual of Requirements and Guidelines |
MRL |
Maximum residue limit |
NCRIS |
National Chemical Registration Information System Database |
NDPSC |
National Drugs and Poisons Schedule Committee |
NHMRC |
National Health and Medical Research Council |
OCS |
Office of Chemical Safety |
OECD |
Organisation for Economic Co-operation and Development |
OGTR |
Office of the Gene Technology Regulator |
OHS |
Occupational health and safety |
OIE |
World Organisation for Animal Health |
PICs convention |
Rotterdam Convention on the Prior Informed Consent Procedure for Certain Hazardous Chemicals and Pesticides in International Trade |
PMF |
Plant master file |
POPs convention |
Stockholm Convention on Persistent Organic Pollutants |
PRS |
Public Release Summary |
SOP |
Standard Operating Procedure |
SPF |
Specific pathogen free |
SUSDP |
Standard for the Uniform Scheduling of Drugs and Poisons |
TAN |
Trade Advice Notice |
TGA |
Therapeutic Goods Administration |
VICH |
International Co-operation for Harmonisation of Technical Requirements for Registration of Veterinary Medical Products |
REVISION HISTORY
| Revision Date | Description of Revision |
|---|---|
| 1 July 2005 | First edition |
| 1 October 2005 | Second edition
|
| 1 April 2006 | Third edition
|
| 1 July 2007 | Fourth edition
|
