This content is current only at the time of printing. This document was printed on 28 July 2021. A current copy is located at https://apvma.gov.au/definition-of-terms/q
You are here
Definition of terms
The potential hazard of a chemical to the environment. It can be determined by dividing the estimated environmental concentration of the chemical by the relevant toxicity concentration. The resulting quotient, Q, then provides a measure of the risk to the organism concerned.
In terms of manufacturing, the action of confirming that any equipment used, or process step applied, in the manufacturing process works correctly and actually leads to the expected results. The qualification process can be applied to equipment installation (installation qualification or IQ), equipment operation under different operating conditions (operational qualification of OQ), or equipment operation as part of a specific process (process qualification or PQ). Validation is often the sum of qualification steps.
The use of a narrative form or descriptive scales to describe the characteristics of, and likelihood of, each event arising and its consequences. An analysis that ascertains the nature of the attributes, behaviour, or opinions of the entity being measured.
Information that is difficult to measure, count, or express in numerical terms.
Research involving detailed, verbal descriptions of characteristics, cases and settings. Qualitative research typically uses observation, interviewing and document review to collect data.
The suitability of either an active constituent or agvet chemical product for its intended use. This term includes attributes such as the identity, strength or purity.
in the conduct of a trial or study
Those procedures and controls, including inspections and audits, that are designed to monitor studies to assure the quality of the data.
The sum total of arrangements made to ensure that products are consistently manufactured in an appropriate manner to the quality standards required for their intended use.
The processes concerned with specifications, sampling and testing and with the organisation, documentation and release procedures that ensure that the necessary and relevant tests are carried out. Quality control ensures that materials are not released for use, nor products released for supply or sale, until their quality has been judged to be satisfactory. Quality control processes are part of a quality assurance system.
|quality control function|
|quality control function||
The procedures carried out by a manufacturer to ensure that effective quality control is carried out at all stages of the manufacturing process and that the finished product meets required specifications.
To attach numbers to an observation.
An analysis that ascertains the magnitude, amount, or size (eg of the attributes, behaviour, or opinions) of the entity being measured.
The use of numerical data to describe the characteristics of, and likelihood of, each event arising and its consequences.
Information that can be expressed in numerical terms, counted, or compared on a scale.
Research that examines a phenomenon through the numerical representation of observations and statistical analysis.
|Quantitative structure activity relationship model (QSAR)||
Quantitative structure activity relationship models are used to relate a set of predictor variables (eg physicochemical properties of a chemical) to response variables (eg biological activity) and may be used to predict values in situations where experimental or analogue data are not available.
The control of import and export of plants, animals and commodities to prevent spread of diseases and pests.
The holding of an imported plant, animal or commodity in isolation for a period to ensure their freedom from pests and diseases.
In terms of manufacturing, the status of starting materials, or intermediate, bulk or finished products that are isolated, whether physically or by a system, while awaiting a decision on their suitability for processing or for sale and distribution.