Checklist Claus Description Example
Record e
Number
1 5.6.1 Management reviews Management review minutes
2 6.2.2 Education, training, skills and experience Training plan, training matrix,
e training records and CVs
3 7.1d Evidence that the realisation processes Project quality plan
and resulting product fulfil requirements
4 7.2.2 Results of the review of requirements Change review
related to the product and actions arising
from the review
5 7.3.2 Design and development inputs relating Customer specifications,
to product requirements design approval logs
6 7.3.4 Results of design and development Design development minutes
reviews and any necessary actions
7 7.3.5 Results of design and development Design plan, test plan
verification and any necessary actions document outputs
8 7.3.6 Results of design and development Test plans, test reports and
validation and any necessary actions acceptance records
9 7.3.7 Results of the review of design and Design review minutes
development changes and any necessary
actions
10 7.4.1 Results of supplier evaluations and any Supplier evaluations,
necessary actions arising from the subcontractor assessments,
evaluations approved supplier list
11 7.5.2 As required by the organization to Schedules of achieved results
d demonstrate the validation of processes
where the resulting output cannot be
verified by subsequent monitoring or
measurement
12 7.5.3 The unique identification of the product, Serial number logs
where traceability is a requirement
Checklist Claus Description Example
Record e
Number
13 7.5.4 Customer property that is lost, damaged Delivery notes, incoming
or otherwise found to be unsuitable for material schedules, defective
use material reports or NCRs
14 7.6a Basis used for calibration or verification Customer specifications,
of measuring equipment where no corporate standards
international or national measurement
standards exist
15 7.6 Validity of the previous measuring Test plan document outputs
results when the measuring equipment
is found not to conform to requirements
16 7.6 Results of calibration and verification of Calibration certificates.
measuring equipment records and calibration logs
17 8.2.2 Internal audit results and follow-up Internal audit report
action
18 8.2.4 Indication of the person(s) authorising Release acceptance record
release of product.
19 8.3 Nature of the product nonconformities Non conformance report,
and any subsequent actions taken, concession report
including concessions obtained
20 8.5.2 Results of corrective action Corrective action reports and
logs
21 8.5.3 Results of preventive action Preventive action reports and
logs
ISO 9001 mandatory procedures
Document control procedure 4.2.3
Control of Records procedure 4.2.4
Internal audit procedure 8.2.2
Control of non-conformance procedure 8.3
Corrective action procedure 8.5.2
Preventive action procedure 8.5.3
ISO 9001 quality system documentation requirements
Quality policy
Quality objectives
A quality manual
Other documents required for effective planning, operation and control
The records specified by ISO 9001
All the ISO 9001 requirements and mandatory procedures are explained in our Quality Manual
Template and guidance document PDF.
>> View Quality Manual Template example
>> View guidance document example
>> Review our Checklist of the 21 records required by ISO 9001:2008
