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GLOSSARY OF TERMS
PART A (Certification)

Part 1 /
Part 2 /
Part 3
The following definitions apply in the context of the Rules of the lEC Quality
Assessment System for Electronic Components (reproduced from annex A, Terms and
definitions, of the Basic Rules of the IECQ-CECC, IEC Publication QC 001001,
with the original numbering).
A.1
quality assessment
the totality of measures carried out consistently and systematically in order to
ensure that a product conforms with the requirements of a stated specification
A.2
participating country
a country in which the National Committee of the IEC, or a body recognized by
the National Committee of the lEC, has been admitted into the System through
having met the participation requirements
NOTE - This term includes all categories of participation outlined in 10.1 to
10.4 of the Basic Rules.
A.3
specification a detailed statement of a set of requirements to be
satisfied by a product, a material or a process, indicating, whenever
appropriate, the procedure by means of which it may be determined whether the
requirements are satisfied
A.4
standard
document, established by consensus and approved by a recognized body, that
provides, for common and repeated use, rules, guidelines or characteristics for
activities or their results, aimed at the achievement of the optimum degree of
order in a given context
[ISO/IEC Guide 2: 1996, definition 3.2]
NOTE - Standards should be based on the consolidated results of science,
technology and experience, and aimed at the promotion of optimum community
benefits.
A.5
applicable standard, or applicable specification a standard, or
specification, applicable to a component, group of components, material, or
process and which has been written in accordance with the Rules of the System,
or such reference standards, or specifications, as have been adopted for use
within the System
A.6
provisional specification
a specification or part thereof, allowed for use temporarily under the System in
the absence of an applicable specification
A.7
detail specification
a document which gives directly, or by making reference to other documents, all
information necessary to completely describe a given component, range of
components or material and to ensure conformance thereof with the requirements
for quality assessment.
A.8
distributor
an organization contractually authorized by one or more manufacturers to store,
re-pack and sell completely finished components from these manufacturers
A.9
independent testing laboratory
an organization wishing to make its services available to other organizations
within the System, which has the facilities and capability to carry out tests
and measurements on electronic components or materials in accordance with their
specification(s) and which is independent of a manufacturer's production
department
A.10
manufacturer of an electronic component
an organization, situated at a stated location or stated locations, that carries
out or controls such stages in the manufacture, inspection, handling and storage
of an electronic component that enables it to accept responsibility for the
quality assessment of that component
A.11
Designated Management Representative (DMR)
a person, acceptable to the National Supervising Inspectorate (NSI), who is a
member of the organization concerned and who is responsible for the quality
system of that organization. This person is the normal means of communication
between the NSI and the organization
A.12
approval of manufacturer
a decision by the National Certification Body (NCB) that a manufacturer has the
organization and the facilities to assure the production and supply of
components in accordance with the requirements of the System, and that the
manufacturer meets the requirements of the System
A.13
approval of distributor
a decision by the NCB that a distributor has the organization and the facilities
necessary to assure the supply of components in accordance with the requirements
of the System
A.14
approval of independent testing laboratory
a decision by the NCB that a testing laboratory is capable of carrying out its
function under the System and is free from any influence which would prevent it
from acting in an impartial manner
A.15
inspection (of components and materials)
the process of selecting samples from an inspection lot; measuring, examining,
testing or otherwise comparing each specimen of these samples with the
requirements of the applicable specification; deciding whether the sample
complies with the applicable specification and what subsequent action shall be
taken with regard to the inspection lot
A.16
quality conformance inspection an inspection carried out by or on behalf
of the manufacturer under the surveillance of an NSI on the components and
materials he manufactures, in order to establish that their quality is being
maintained in accordance with the requirements of the applicable specification
A.17
release
a decision, taken in accordance with the Rules of the System1 that an inspection
lot has successfully passed all the relevant requirements of the applicable
specification(s)
A.18
measurement standard
an instrument, a device, or a material of known characteristics used to
establish and maintain the integrity of measuring equipment or measuring methods
NOTE - Measurement standards are classified in different levels, for example,
reference, transfer.
A.19
specialist contractor
a contractor providing a specialist process capability or technical service to
the electronic components industry

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