CMA Intermediate · Corporate Accounting and Auditing
Audit Sampling, Audit Techniques and Analytical Procedure: formula sheet
Key formulas
- Audit sampling
- Procedures on < 100% of items, with every sampling unit having a chance of selection
- Purpose: a reasonable basis for conclusions about the whole population (SA 530, para 5(a)).
- Statistical sampling
- Random selection + probability theory to evaluate results
- If either feature is missing, it is non-statistical sampling.
- Evaluation of tests of details
- Projected misstatement + anomalous misstatement (if any) compared with tolerable misstatement
- If the total exceeds tolerable misstatement, the sample does not give a reasonable basis for conclusions about the population. The closer it is to tolerable misstatement, the more likely actual misstatement exceeds it (para A22).
- Tolerable misstatement
- Tolerable misstatement ≤ performance materiality
- It may be equal to or lower than performance materiality (para A3).
- Sample size factors (tests of details)
- Increase: assessed risk of material misstatement, desired assurance, expected misstatement. Decrease: tolerable misstatement, other substantive procedures on the same assertion, stratification. Population size: negligible effect
- From Appendix 3. For large populations, size has little effect.
- Sample size factors (tests of controls)
- Increase: reliance on controls, expected deviation rate, desired assurance. Decrease: tolerable deviation rate. Population size: negligible effect
- From Appendix 2.
- Sampling interval (systematic selection)
- Sampling interval = Population size ÷ Sample size
- Pick a random starting point within the first interval, then take every item at that interval. Example: 2,000 items and a sample of 40 give an interval of 50.
- Statistical sampling test
- Statistical sampling = Random selection + Probability theory to evaluate results
- Both conditions are needed. Random selection with judgmental evaluation is non-statistical.
- Stratified sample coverage
- Items per stratum = Sample size × (Stratum size ÷ Population size), when sampling in proportion
- Proportional allocation is one option. Auditors often test all high-value items and sample the rest.
- Sampling risk
- Sampling risk = risk that the conclusion from the sample differs from the conclusion if the whole population were tested
- It arises in both approaches but can be quantified only in statistical sampling.
- Simple projection of misstatement (ratio method)
- Projected misstatement = (Misstatement found in sample ÷ Value of sample) × Value of population
- A common way to apply the para 14 requirement when the misstatement is proportional to value. Use it for the population from which the sample was drawn.
- Projection by average error (difference method)
- Projected misstatement = (Misstatement found ÷ Number of items in sample) × Number of items in population
- Useful when errors do not depend on the size of the item. State clearly which method you used.
- Sample deviation rate (tests of controls)
- Sample deviation rate = Number of deviations found ÷ Sample size
- Compare with the tolerable rate you set. The sample rate is the auditor's best estimate for the population rate.
- SA 530 requirement on size
- Sample size must reduce sampling risk to an acceptably low level
- Para 7. Size comes from a statistical formula or professional judgment.
- SA 530 requirement on selection
- Every sampling unit in the population must have a chance of selection
- Para 8.
- Techniques to remember
- Inspection, Observation, External confirmation, Recalculation, Reperformance, Analytical procedures, Inquiry
- These are the procedures SA 500 describes for obtaining evidence. Write them in this order to avoid missing any.
- Strength of evidence
- External and auditor-generated evidence > internal evidence; documents > oral statements
- Evidence from independent sources and obtained directly by the auditor is more reliable. Use this to explain why inquiry alone is not enough.
- Choice of testing approach
- Strong internal control → smaller test checks; weak internal control → larger tests or complete checking
- Complete checking is also used for small populations or high-risk items.
- Difference to investigate
- Difference = Recorded amount − Expected amount
- Investigate if the difference is larger than the threshold you set. A small difference may still matter if the area is high risk.
- Gross profit ratio
- Gross profit ratio = (Gross profit ÷ Net sales) × 100
- A sudden change may signal sales or closing stock errors, or a change in pricing or product mix.
- Current ratio
- Current ratio = Current assets ÷ Current liabilities
- Useful for going concern and liquidity concerns.
- Debtors turnover period
- Average collection period (days) = (Trade receivables ÷ Credit sales) × 365
- A rising period may point to overstated receivables or weak recoveries.
- Trend (percentage change)
- Change % = (Current year − Previous year) ÷ Previous year × 100
- Compare with the change you expect from business facts.
- Choice of procedure (SA 520, A4)
- Tests of details, substantive analytical procedures, or both
- Chosen by judgment on expected effectiveness and efficiency in reducing audit risk to an acceptably low level.
- When analytical procedures are less suitable (SA 520, A9)
- Weak controls → rely more on tests of details
- Example in SA 520: weak controls over sales order processing mean more reliance on tests of details for receivables.
- Audit software
- Auditor's program + client's real data → exceptions, totals, samples
- Tests the data. Used for substantive tests such as recalculation, ageing, duplicates, gaps and sample selection.
- Test data
- Auditor's dummy transactions + client's program → compare actual output with expected output
- Tests the program controls. Include both valid and invalid transactions. Run it on a copy or under controlled conditions so live records are not corrupted.
- Core difference
- Audit software = tests data; Test data = tests processing logic
- This is the usual one-line answer for the comparison question.
- Other CAAT forms
- Integrated test facility; parallel simulation; embedded audit module; data analytics
- Name these for completeness, with one line on each.
Quick revision
- Audit sampling means applying procedures to fewer than 100% of items so every unit has a chance of selection.
- Sampling risk is the risk that the conclusion from the sample differs from testing the whole population.
- Non-sampling risk arises from causes unrelated to sample size, such as wrong procedures or misreading evidence.
- Tolerable error is the maximum error the auditor accepts in the population.
- An anomaly is an error shown to be not representative of the population.
- Statistical sampling uses random selection and probability theory to evaluate results; otherwise it is non-statistical.
- A larger sample is needed when risk is higher or tolerable error is lower.
- Project the errors found in the sample to the population before drawing a conclusion.
- Selective testing checks chosen items, but unlike sampling its results are not projected statistically to the whole population.
- Analytical procedures are used in risk assessment, as substantive procedures and in the overall final review.
- Unusual fluctuations found by analytical procedures need investigation and corroborating evidence.
- CAATs use software to test data, and they depend on reliable data and proper controls.
Common mistakes
- Saying sampling means testing a random selection only Fix: Random selection is needed for statistical sampling only. Audit sampling requires that every unit has a chance of selection. Non-statistical sampling is also valid sampling.
- Treating non-sampling risk as controllable by a bigger sample Fix: Non-sampling risk comes from inappropriate procedures, misinterpreting evidence or failing to recognise errors. Training, supervision and good procedures reduce it, not a larger sample.
- Calling any random selection statistical sampling. Fix: Remember both features: random selection and probability-based evaluation. Missing either one makes it non-statistical.
- Treating haphazard selection as random selection. Fix: Random uses a method such as random numbers, giving every item a known chance. Haphazard has no structure and relies on the auditor avoiding bias, so it is non-statistical.
- Counting every difference found as a misstatement. Fix: Define the misstatement first. In a receivables existence test, a payment received just after the confirmation date is not a misstatement.
- Saying the projected misstatement is the amount the client must book. Fix: State that projection gives a broad view of the scale of misstatement and may not be sufficient to determine an amount to be recorded.
- Confusing recalculation with reperformance. Fix: Recalculation checks arithmetic accuracy. Reperformance redoes a procedure or control, such as a reconciliation or an approval check.
- Treating observation as proof of year-round operation. Fix: State the limitation and say the auditor supports it with other procedures.
- Treating analytical procedures as only a ratio calculation. Fix: Always add the expectation, the investigation of differences and the audit conclusion.
- Forgetting that analytical procedures are used at three stages. Fix: List risk assessment, substantive procedures and final review whenever the question asks about use.
Exam tips
- Learn the SA 530 definitions word for word in your own plain phrasing; short notes questions reward them.
- For sampling risk versus non-sampling risk, give a definition, two examples each and one line on whether sample size affects it.
- In sums, show the line: projected plus anomalous misstatement versus tolerable misstatement, then state the conclusion.
- Remember the direction of each sample-size factor; MCQs often ask whether a factor increases or decreases sample size.
- There is no negative marking in Section A, so attempt every MCQ.
- For difference questions, set out a two-column comparison: selection method, evaluation method, sampling risk measurement, cost and skill needed.
- In numerical questions, always show the sampling interval formula and the random start before listing items.
- For suitability questions, link the method to the population: stratified for varied values, systematic for numbered uniform items, block only with caution.