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This is Part 4 of the article, where we are discussing the different phases of the validation processes an RTO should be following to ensure they meet regulatory requirements and industry expectations.
In the previous articles, we discussed the following regarding the validation of assessment resources:
In this month’s article, we will explore the following:
Why do you need to keep validators information?
You need to keep for validators information for the following reasons:
Reasons why validation of assessment and learner resources should be systematic and ongoing.
A unit of competency needs to be regularly reviewed to ensure that it meets current industry and regulatory requirements, therefore, you must have a systematic and ongoing mechanism to track any changes and to ensure all your resources are up-to-date and current.
How to schedule validation
The first step is to develop a “validation schedule” used to validate each training product (AQF qualification, skill set, unit of competency, accredited short course and module) on your scope of registration.
A validation schedule is a five year plan and each training product must be reviewed at least once in that five-year period, and at least 50% of your training products must be validated in the first three years of the schedule. Your RTO might choose to validate its training products more often, for example, if risk indicators demonstrate that more frequent validation is required. Indicators of risk might include:
Once you have your validation schedule you need to complete a validation plan with dates and timelines. The more detailed your plan is with regards to the who (needs to be included), when (what date and for how long), and what (which units is being validate, what information will be needed, from where are we getting it) the better your outcomes for your validation will be.
What is statistically valid sampling?
A statistically valid sample is one that is:
Use ASQA’s validation sample size calculator for more information. It can be found here:
Validation outcomes
You must keep all records as a soft-copy/scanned format or in hard-copy. The records must include all the tools used to conduct validation such as assessment resources, validation forms and checklists, profiles of validators etc.
The validation outcomes should identify recommendations for improvement to the assessment tool, assessment process or assessment outcome.
Sometimes the validation outcome can identify critical issues in the collection of valid evidence.
When this occurs, you may:
Your validation plan must clarify how you will document and act on validation outcomes. For example, an assessment validation checklist addressing the principles of assessment and rules of evidence may be utilised to document the validation outcomes. Outcomes of validation may be acted upon through your RTO’s continuous improvement processes.
Your RTO must have a records management process to retain the evidence of the validation. You should retain evidence of:
If the validation outcomes recommend improvements to the assessment tool, you should implement these recommendations across all training products, not only those included in the sample. If you make changes to the assessment tool, complete quality checks and review the revised tool prior to implementation.