Module 10.3 Testing of Reliability
Module 10.3 Testing of Reliability
ToC
Materiality
Risk assessment and Accept-reject
response sampling
U
n
d
e Risk Register
r
Lead schedule
s SToD: Testing
SToD: Approach &
t single/once off
accumulation per target
a achievements
n
SToD: Testing
d
C,M,R,P&D
i
n SToD: Testing per
SToD: Testing per
popultation
g
population
Adjustments
Overall
Conclusion Evaluation of uncorrected misstatements and concluding
summary
For SM per indicator For SM per target Per target Per population per assertion
①
Reliability assertions and
audit criteria
Reliability assertions and audit criteria
Reliability
Assertions
Substantive/
• Validity
combined approach
• Accuracy
• Completeness
Pertaining to actual performance/target
achieved
• Combined vs substantive
Size 3
Tests of details
Size 2 Size 2
Substantive analytical Substantive analytical
procedures procedures
Tests of details
Tests of
Tests of controls controls
Test of Substantive
Controls Procedures
Substantive
Test of
Analytical
Detail
Procedures
Nature of audit procedures
• Can CAATS be used?
• To what extent can CAATs be used in designing
and executing test of details:
Perform more extensive testing of electronic files
Select sample events/occurrences/items/transactions
from key electronic files
Sort events/occurrences/items/transactions with
specific characteristics
Test an entire population instead of a sample.
• ISA involvement
Direction of testing
Performance records Source documents
Validity
Accuracy Using highest
level of
Validity and Accuracy assurance
required
Completeness
Primary vs
secondary
Substantive analytical procedures for
AoPO
Approach with care
• Suitable?
• Able to predict outcome of target?
• Logical relationship between the recorded value
and the data to be used to predict
• Plausible and predictable?
• Less effective when testing target subject to
management discretion
②
Basic risk response rules
Reliability
Basic risk response rule
Reliability
• Further audit procedures in responsive to risk of MM
• More persuasive audit evidence
• Circumstances appropriate for ToC
• SP’s for all material performance indicator/measure
and targets
• SP’s for significant risk SToD if fully substantive
approach
• Special procedures
Special consideration items
Performance information closing process
Rule 1 -
Further audit procedures responsive to
assessed risk of MM
• Further audit procedures responsive to the
assessed risks of material misstatement at
the assertion level; referring to the validity,
accuracy and completeness
TARGET
Size 3
proedures
Tests of details
Size 2 Size 2
Substantive analytical Substantive analytical
Tests of details procedures
3 Significant
2 Standard
1 Minimal
Rule 3 –
Are test of controls appropriate?
Similar to AFS
Rule 4 –
Always SPs for material performance
measure/ indicator and targets
ALL material NB
Also test ALL non-
performance indicators
material indicators and
and related targets are
related targets
tested
Testing of non-material indicators
Always: Required procedures
relevant to performance
information closing process (rule 7)
The likelihood
NO significant
NO prior year due to other
risk indicators
misstatements risk factors is
are present
LOW
Rule 5 –
Specific SP’s for significant risk
3 Significant
• Auditor’s response must include substantive
procedures specifically responsive to risk
• If substantive approach followed, must include
test of details
Rule 6 –
Specific SP’s for specific consideration
items
• When a measure/indicator and any of its targets
is affected by identified special consideration,
perform required procedures
• Specific consideration?
Auditing of estimates
Using the work of internal auditors
Using the work of an auditor’s expert
Using the work of “others”
Rule 7 –
Performance information closing process
NB
SP’s related to the collation, summary and finalisation
of information on actual target achievement
a) Agree/reconcile the reported information with
underlying records
b) Examine adjustments to the reported information
on target achievement in the process of collating,
summarising and closing-off
Lead schedule
Roll forward rules
Interim test performed
Accept – Reject
Accept-reject sampling for tests of
details
⑤
Means for selecting items
for testing
Selection hierarchy
Selecting all items
•
Selecting specific items only
ToC
Materiality
Risk assessment and Accept-reject
response sampling
U
n
d
e Risk Register
r
Lead schedule
s SToD: Testing
SToD: Approach &
t single/once off
accumulation per target
a achievements
n
SToD: Testing
d
C,M,R,P&D
i
n SToD: Testing per
SToD: Testing per
popultation
g
population
Adjustments
Overall
Conclusion Evaluation of uncorrected misstatements and concluding
summary
For SM per indicator For SM per target Per target Per population per assertion
Selecting all items
• Target is measured as a single/ once-off
achievement SToD: Testing per
population (Tab A)
• Target = 0
• Numbers, percentages, values, etc.
• Small number of items
• Significant risk with no other means of
testing
• CAATS
• Factual misstatements
Selecting specific items
5.0%
(10% x 50%) 60 40 20
7.5%
(10% x 75%) 40 27 14
Step 2 – Select the sample items
Disagreement:
Difference between information on actual performance supported by the
audit evidence and information as reported by the auditee
Limitation:
Audit evidence not available or not adequate
uncertain whether or not item is misstated
Performance Overall
materiality materiality
5% / 7.5% 10%
ToC
Materiality
Risk assessment and Accept-reject
response sampling
U
n
d
e Risk Register
r
Lead schedule
s SToD: Testing
SToD: Approach &
t single/once off
accumulation per target
a achievements
n
SToD: Testing
d
C,M,R,P&D
i
n SToD: Testing per
SToD: Testing per
popultation
g
population
Adjustments
Overall
Conclusion Evaluation of uncorrected misstatements and concluding
summary
For SM per indicator For SM per target Per target Per population per assertion
6
Accumulation and evaluation
of misstatements for
reliability
Accumulating reliability misstatements
Net
Communicate uncorrected
Adjustments by Audit
all misstatements
management? adjustments
misstatements – calculate the
MOR per target
Calculate misstatement occurrence
rate
• Calculate MOR based on the total uncorrected
misstatement for the target – i.e. the net effect of all
uncorrected misstatements SToD: Approach
and accumulation
• Using the applicable formula
– Single / once-off achievement - 0% or 100%
– R-value/Numbers - Total uncorrected
misstatement/ Total misstatement
– Percentage / rate - Total uncorrected
misstatement / Reported achievement as
percentage
Programme/objective/development priority: [Provide description]
Audited value for
Performance Actual reported the target Total
measures/indicators performance uncorrected Misstatement
and their targets in the APR misstatements occurrence rate
(i.e. “Book identified for
value”) the target *Note 1*
Material measures/indicators and their related targets
Measure/indicator #1: [Provide description]
1.1 98% 87% 11% 11.2%
[Describe target] *Note 2*
ToC
Materiality
Risk assessment and Accept-reject
response sampling
U
n
d
e Risk Register
r
Lead schedule
s SToD: Testing
SToD: Approach &
t single/once off
accumulation per target
a achievements
n
SToD: Testing
d
C,M,R,P&D
i
n SToD: Testing per
SToD: Testing per
popultation
g
population
Adjustments
Overall
Conclusion Evaluation of uncorrected misstatements and concluding
summary
For SM per indicator For SM per target Per target Per population per assertion