Changes in New Standard ISO 9001:2015 - Documented Information
Documented
information is the information required to be controlled and maintained by an
organization and the medium on which it is contained.
Note 1:
Documented information can be in any format and media and from any source.
Note
2: Documented information can refer to:
- the
quality management system, including related processes;
-
information created in order for the organization to operate (documentation);
- evidence
of results achieved (records).
Structure and Terminology
There is no
requirement for the terms used by an organization to be replaced by the terms
used in ISO 9001:2015 to specify quality management system requirements.
Organizations can choose to use terms which suit their operations, e.g.,
records, documentation, protocols, etc. rather than documented information.
Documented Information
As part of
the alignment with other management system standards, a common clause on
Documented Information has been adopted without significant change or addition.
Where appropriate, text elsewhere in ISO 9001:2015 has been aligned with its
requirements. Consequently, the terms documented procedure and record have both
been replaced throughout the requirements text by documented information.
Where ISO
9001:2008 would have referred to documented procedures (e.g., to define,
control, or support a process), this is now expressed as a requirement to
maintain documented information.
ISO 9001:2015 - Required Documents
Number
|
“Maintain” as Documented Information
|
ISO 9001
|
01
|
Documented information stating the scope of
quality management system
|
4.3
|
02
|
Documented information to
extent necessary to support operation of processes
|
4.4
|
03
|
Documented information available for quality policy
|
5.2.2.a
|
04
|
Documented information required by this International Standard
|
7.5.1.a
|
05
|
Documented information determined by the organization as being necessary for
the effectiveness
of the quality management system
|
7.5.1.b
|
06
|
Documented information of
external origin determined by the organization to be
necessary for
the planning and
operation of
the quality management
system
|
7.5.3.2
|
Where ISO
9001:2008 would have referred to records, this is now expressed as a requirement
to retain documented information.
ISO 9001:2015 - Required Records
Number
|
“Retain” as Documented
Information
|
ISO 9001
|
01
|
Documented information to extent necessary
to have confidence that processes
are being carried out as
planned
|
4.4
|
02
|
Documented information on the quality objectives
|
6.2.1
|
03
|
Documented information as
evidence
of fitness for
purpose of monitoring and
measurement
resources
|
7.1.5
|
04
|
Documented information on basis
used for calibration or verification where
no
such standards exist
|
7.1.5
|
05
|
Documented information as
evidence
of competence
|
7.2.d
|
06
|
Documented information required by this International Standard
|
7.5.1.a
|
07
|
Documented information determined by the organization as being necessary for
the effectiveness
of the quality management system
|
7.5.1.b
|
08
|
Documented information to the extent necessary to have confidence that the
processes have been carried out as planned
|
8.1.e
|
09
|
Documented information to the extent necessary to demonstrate conformity of
products and services to requirements
|
8.1.e
|
10
|
Documented statement of customer requirements
(or confirmation)
|
8.2.3
|
11
|
Documented information on results of
requirements review
|
8.2.3
|
12
|
Documented information to confirm that design and
development
requirements
have been met
|
8.3.2.g
|
13
|
Documented information resulting from the
design and development process
|
8.3.5
|
14
|
Documented information on design and
development changes
|
8.3.6
|
15
|
Documented information on the results of the evaluations, monitoring of
the
performance, and re-evaluations of the external providers
|
8.4.1
|
16
|
Documented information that defines the characteristics of the products and
Services
|
8.5.1.a
|
17
|
Documented
information that defines the
activities to be performed
and the
results to be achieved
|
8.5.1.b
|
18
|
Documented information necessary to maintain traceability
|
8.5.2
|
19
|
Documented information describing the results of the review of
changes,
the personnel authorizing the change,
and any necessary actions
|
8.5.6
|
20
|
Documented information to provide traceability
to the person(s) authorizing
release of products
and services for delivery to the customer
|
8.6
|
21
|
Documented information of
actions taken on nonconforming process
outputs,
products and services, including on any concessions obtained and
on the person or
authority that made the decision regarding dealing with
the nonconformity
|
8.7
|
22
|
Documented information as evidence
of the results of monitoring and
measurement
activities
|
9.1.1
|
23
|
Documented information as
evidence of the
implementation of
the audit
program and the audit results
|
9.2.2.f
|
24
|
Documented information as
evidence of the
results of management reviews
|
9.3.2
|
25
|
Documented information as evidence
of the nature of the
nonconformities
and
any subsequent actions
taken
|
10.2.2.a
|
26
|
Documented information as
evidence of the
results of any corrective action
|
10.2.2.b
|
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