2008 changes to ISO 9001
Overview
Every few years all international standards are reviewed to ensure their continued relevance.
ISO 9001 underwent a major overhaul in 2000 and another revision was issued in November 2008.
The changes are minimal and provide further clarification of the clauses rather than additional requirements.
More detailed information can be viewed on the
ISO website.
To obtain a personalized quotation for audit to the ISO 9001 standard click here.
Existing ISOQAR Customers
ISOQAR customers have until the 14th November 2010 to comply with the changes.
However, if a re-assessment is due before then, but after 14th November 2009, it must be against the new standard.
Guidance and support will be provided during surveillance visits or by telephone.
Below you will find a checklist of the changes we have identified and intend to audit against.
New Customers
Before 15th November 2009 (a year after the issue of ISO 9001: 2008) new customers can choose to be audited against either the 2000 or 2008 version of ISO 9001. After this date all new audits will be against ISO 9001: 2008.
However, new customers are encouraged to opt for the new standard straightaway.
More information can be found on the International Accreditation Forum's website.
The salient information is towards the end of the article.
Obtaining a copy of ISO 9001: 2008
The standard itself is copyright so we are unable to distribute it.
You can buy or download it from a variety of sources including
The Stationery Office and
ISO itself.
Search for "ISO 9001 requirements" not just "ISO 9001" to locate the standard more readily.
ISO 9001: 2008 Checklist
The 2008 version of the standard has no requirements additional to the 2000 edition it replaces.
It merely provides clarification to the existing requirements.
Here is a summary of the changes we have identified: (also available here as a pdf )
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Clause
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Clarification
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Addressed?
Yes / No
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Does
the company have a copy or access to a copy of ISO 9001: 2008?
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Have
all references been amended to reflect an upgrade to ISO 9001: 2008?
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4.1
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Confirm
that any outsourced process is fully controlled where there is potential for
an impact on the product or service provided. This should be controlled through clause
7.4. The type and extent of control
should be defined.
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5.5.2
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Confirm
that the Management Representative is a member of the organisations own management.
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6.2.1
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Ensure
that any person performing work affecting "conformity of the product/service" is competent.
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6.3
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Include
information systems as a supporting service.
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6.4
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Confirm
that all applicable work environment conditions have been considered.
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7.2.1
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Ensure
any post delivery activity is covered (e.g. warranty, recycling, disposal
obligation).
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7.3.1
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Design
review, verification and validation have distinct purposes. Confirm that they have been conducted and
recorded as suitable for the product or the organisation.
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7.3.3
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Ensure
that the preservation of the product has been considered as applicable.
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7.5.4
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Personal
data and intellectual property (e.g. software) may now be considered as
customer property and reported if unsuitable, lost or damaged.
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7.6
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Title
amended. "Control of monitoring and measuring equipment."
Confirmation
that computer software may not be subject to traditional calibration. May be focused on verification and
configuration management.
Calibration
status identification does not have to be physically on the equipment,
provided that the identification employed can determine the calibration
status.
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8.2.2
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Ensure
that the Management of the "units" audited have implemented correction and
corrective actions.
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8.2.3
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Confirm
that appropriate monitoring and measurement processes have been implemented,
dependant on the impact of the product/service and the effectiveness of the management
system.
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8.2.4
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The
standard specifies that when products are released to the customer the company
must maintain records of who is
responsible to sign off the product for delivery.
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8.3
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Corrective
action taken should be appropriate to the effects, or the potential effects
of the nonconformity when nonconforming product is detected AFTER delivery or
use has started.
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8.5.2
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Review
of the effectiveness of corrective
actions taken.
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8.5.3
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Review
of the effectiveness of
preventative actions taken.
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