ISO9001 2015 Checklist
ISO9001 2015 Checklist
ISO9001 2015 Checklist
SYSTEMS - REQUIREMENTS
SELF-ASSESSMENT CHECKLIST
4.1
4.2
UNDERSTANDING THE
INTERESTED PARTIES
(a)
(b)
(a)
(b)
4.3
NEEDS
AND
EXPECTATIONS
OF
Have we determined what interested parties are relevant to the QMS and
what are their requirements
Do we monitor and review this
4.4
5.1
5.1.2
CUSTOMER FOCUS
5.2
QUALITY POLICY
5.3
6 Planning
TO ADDRESS RISKS AND OPPORTUNITIES
6.1 ACTIONS
Have we determined the risks and opportunities that need to be addressed to:
(a)
(b)
(c)
6.2
6.3
Have we planned:
(a)
actions to address these risks and opportunities
(b)
how to integrate these actions into the QMS
6.2.1
6.2.2
PLANNING OF CHANGES
7 Support
7.1 RESOURCES
7.1.1 General
Have we determined and provide the resources needed for the
7.1.2
QMS?
Have we considered
(a)
the capabilities of, and constraints on existing resources
(b)
what needs to be obtained from external providers
People
7.1.3
Infrastructure
7.1.4
7.1.5
7.1.6
ORGANIZATIONAL KNOWLEDGE
7.2
COMPETENCE
7.3
AWARENESS
7.4
COMMUNICATION
Do we
(a)
determine the necessary competence of person(s) that could affect the
QMS
(b)
ensure that these person(s) are competent on the basis of appropriate
education, training, or experience
(c)
take actions to access the necessary competence where applicable
(d)
retain appropriate documented information as evidence of competence
Have we ensured that person(s) doing work under the control of our business
are aware of
(a)
the quality policy and relevant quality objectives
(b)
their contribution to the effectiveness of the QMS, including the benefits
of improved quality performance
(c)
the implications of not conforming with the quality management system
requirements
Have we determined the internal and external communications relevant to the QMS
including:
(a)
what will be communicated
(b)
when to communicate
(c)
with whom to communicate
(d)
how to communicate
(e)
Who communicates
7.5
DOCUMENTED INFORMATION
7.5.1
General
Do we ensure we have
(a)
identification and description (such as a title, date,
author, or reference number)
(b)
review and approval
7.5.2
7.5.3
Do we ensure we have
(a)
identification and description (such as a title, date,
author, or reference number)
(b)
review and approval
8 Operation
PLANNING AND CONTROL
8.1 OPERATIONAL
Have we planned, implemented and controlled our processes
Have we
(a)
determined the requirements for our products and services
(b)
established criteria for the processes and the acceptance of products and
services
(c)
determined the resources needed
(d)
implemented controls
(e)
retained documented information as necessary to demonstrate processes
have been carried out effectively and product conformance
(f)
planned changes and reviewed issues,
(g)
ensured that outsourced processes are controlled
8.2
8.2.1
Customer communication
8.2.2
8.3
8.2.3
8.2.4
Have we
(a)
ensured that documented information is amended and
that relevant personnel are made aware of the changed
requirements when requirements for products and services
are changed
8.3.1
General
8.3.2
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8.3.3
8.3.4
8.3.5
Have we considered:
(a)
functional and performance requirements
(b)
similar designs
(c)
statutory and regulatory requirements
(d)
standards or codes of practice
(e)
potential consequences of failure due to the nature of the products
and services
Have we ensured inputs are adequate, complete, and unambiguous and
all conflicts are resolved
Have we retained documented information on design and development
inputs
Do our controls ensure
(a)
the results to be achieved are defined
(b)
reviews are conducted to ensure designs will meet requirements
(c)
verification is conducted to ensure that design outputs will meet the
defined inputs
(d)
validation ensures products and services are capable of meeting the
specified requirements or intended use
(e)
actions are taken on problems
(f)
documented information of these activities is retained.
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8.3.6
8.4
8.4.1
General
8.4.2
Do we
(a)
ensure externally provided processes are controlled within
our QMS
(b)
define controls over the process and the output
(c)
consider impacts to meet statutory and client requirements
(d)
determine verification requirements
ISO 9001:2015 Quality Management Systems
Requirements Self-Assessment Checklist
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8.4.3
8.5
8.5.1
8.5.2
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8.5.3
8.5.4
Preservation
8.5.5
Post-delivery activities
8.5.6
Control of changes
Do we review and control changes in production to ensure
continuing conformity with requirements
Do we retain documented information of the review of changes
to production including authorisation and any necessary actions
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8.6
8.7
Do we ensure product that does not conform to requirements are identified and
controlled to prevent their unintended use or delivery
Do we take appropriate corrective action
Do we deal with nonconforming products in one or more of the following
ways:
(a) correction
(b)
segregation, containment, return or suspension of production
(c)
informing the customer
(d)
obtaining authorization for acceptance under concession
Do we re-verify when products are corrected?
Do we retain documented information describing the non-conformance, actions
taken, concessions obtained and authorisations
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9 Performance Evaluation
9.1 MONITORING, MEASUREMENT, ANALYSIS AND EVALUATION
9.1.1
9.1.2
General
Have we determined
(a)
what needs to be monitored and measured
(b)
the methods
(c)
when monitoring and measurement is to be done
(d)
when results will be analysed and evaluated
Do we evaluate the effectiveness of the QMS
Do we retain documented information of this
Customer satisfaction
Do we monitor customer perceptions
(this can include customer satisfaction surveys, customer
feedback, market-share analysis, compliments, warranty claims
and dealer reports)
Have we determined how we will obtain, monitor and review this
information
9.1.3
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9.2
INTERNAL AUDIT
9.2.1
9.2.2
Have we:
(a)
planned and implemented an effective audit program
(b)
defined the criteria and scope for each audit
(c)
selected auditors to ensure objectivity and impartiality
(d)
ensured that the results are reported to relevant
management
(e)
taken necessary correction and corrective actions without
undue delay
(f)
retained documented information
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9.3
MANAGEMENT REVIEW
9.3.1
9.3.2
9.3.3
(a)
the status of actions from previous management reviews
(b)
changes in external and internal issues relevant to the
QMS
(c)
information on the QMS including
customer satisfaction and stakeholder feedback
quality objectives performance
product performance and conformity
nonconformance and corrective action
monitoring and measurement including audits
external providers
process performance and conformity of products
and services;
(d)
adequacy of resources
(e)
actions taken regarding risk and opportunity
(f) improvement
Outputs
(a)
opportunities for improvement
(b)
changes to the QMS
(c) resources
Do we retain documented information as evidence of the results
of management reviews
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10 Improvement
10.1
GENERAL
10.2.2
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10.3
CONTINUAL IMPROVEMENT
Do we
(a)
continually improve the effectiveness of the QMS
(b)
consider the outputs of analysis and management reviews to
identify opportunities for continual improvement
(c)
encourage Compass Assurance Services to keep improving and
remain a valuable partner to us
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