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