This content is current only at the time of printing. This document was printed on 28 March 2017. A current copy is located at http://apvma.gov.au/node/316
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The risk analysis process
An application to the APVMA for active constituent approval or product registration typically contains a number of distinct parts, including data for chemistry and manufacture, toxicology relating to public health and occupational health and safety (OHS), residues, environmental safety, and product efficacy. The APVMA and its external advisory agencies perform risk assessments of various parts of the application, assessing both hazard (ie. the intrinsic toxicity of the chemical) and the likely extent of exposure to the chemical.
These assessments determine how toxic a chemical or product is (to humans and to plants and animals in the environment) and the extent to which people, plants or animals are likely to be exposed to the chemical when it is used according to the proposed label.
The APVMA uses these assessments to determine whether the risks associated with the proposed use(s) are acceptable and whether any identified risks can be appropriately managed or mitigated.
The potential risks involved in using a chemical product are communicated to relevant people, such as end users. One of the most important tools for risk communication is the product label that is attached to the product container.
The processes of risk assessment, risk management and risk communication are all part of the risk analysis process.