Примери за използване на Conformity assessment на Английски и техните преводи на Български
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
Authorities conformity assessment.
Conformity assessment procedures 1.
Derogation from the conformity assessment procedures.
Conformity Assessment Programmes(CAP).
Exceptional derogations of the conformity assessment procedures.
Хората също превеждат
This Conformity Assessment Program.
ERTMS group of notified conformity assessment bodies.
This Conformity Assessment Programme.
Involvement of notified bodies in conformity assessment procedures.
Conformity assessment procedures(modules).
Why use CE-marking conformity assessment services from SGS?
Conformity assessment procedure for apparatus.
Supporting quality infrastructures and conformity assessment authorities.
Article 9 Conformity assessment procedures.
Tools for quality infrastructure institutions and conformity assessment bodies.
Conformity assessment procedures for lifts.
Conformity assessment bodies and notified bodies 73.
Certification of management systems is a third-party conformity assessment activity.
Conformity assessment bodies(NANDO): Countries Australia.
The previous version of the regulation did not include conformity assessment processes and modules.
The conformity assessment procedures are set out in Annex III.
Laboratory accredited by China National accreditation service for conformity assessment.
The conformity assessment procedures are set out in Annex II.
Additionally, SZUTEST cannot be directly connected to other competitive products(competitive brand or producer) throughout the conformity assessment process.
The conformity assessment procedure, including CE marking, comprises.
SZUTEST does not engage in any activities that can contradict with the independence of its decisions andevaluations regarding its conformity assessment activities.
List of approved conformity assessment bodies designated by New Zealand.
Conformity assessment tasks include testing, certification and inspection.
Whereas the list of in vitro diagnostic medical devices to be subjected to third-party conformity assessment needs updating, taking account of technological progress and of developments in the field of health protection;