Common use of PROCEDURES FOR DESIGNATING CONFORMITY ASSESSMENT BODIES Clause in Contracts

PROCEDURES FOR DESIGNATING CONFORMITY ASSESSMENT BODIES. The procedures to be followed by New Zealand in designating Conformity Assessment Bodies to assess products against the European Community’s requirements The procedures to be followed by the European Community in designating Conformity Assessment Bodies to assess products against New Zealand’s requirements The Conformity Assessment Bodies listed in Section II will meet the requirements of the Directives listed in Section I, taking into account Council Decision 93/465/EEC of 22 July 1993 concerning the modules for the various phases of the conformity assessment procedures and the rules for the affixing and use of the CE conformity marking, which are intended to be used in the technical harmonisation directives and be designated on the basis of the procedures defined in the Annex to the Agreement. This may be demonstrated through: (a) Inspection Bodies operating according to the requirements of EN 45004 or ISO Guide 39, and either: 1. The procedures for designating conformity assessment bodies will be consistent with the principles and procedures set out in the Annex to the Agreement. 2. The following procedures are deemed to be consistent with those set out in the Annex to the Agreement: Testing Laboratories: — accredited by accreditation bodies which are signatories to the European cooperation for Accreditation (EA) Multilateral Agreement on Calibration and Testing, or — accredited by the Testing Laboratory Registration Council of New Zealand, or — recognised within the IECEE CB Scheme, or — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement. — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement.

PROCEDURES FOR DESIGNATING CONFORMITY ASSESSMENT BODIES. The procedures to be followed by New Zealand in designating Conformity Assessment Bodies conformity assessment bodies to assess products against the European Community’s requirements The procedures to be followed by the European Community in designating Conformity Assessment Bodies conformity assessment bodies to assess products against New Zealand’s requirements The Conformity Assessment Bodies conformity assessment bodies listed in Section II will meet the requirements of the Directives listed in Section I, taking into account Council Decision 93/465/EEC of 22 July 1993 concerning the modules for the various phases of the conformity assessment procedures and the rules for the affixing and use of the CE conformity marking, which are intended to be used in the technical harmonisation directives and be designated on the basis of the procedures defined in the Annex to the Agreement. This may be demonstrated through: (a) Inspection Product Certification Bodies operating according to the requirements of EN 45004 45011 or ISO Guide 39Guides 28 and 40, and either: 1. The procedures for designating conformity assessment bodies will be consistent with the principles and procedures set out in the Annex to the Agreement. 2. The following procedures are deemed to be consistent with those set out in the Annex to the Agreement: (a) Testing Laboratories: — accredited by accreditation bodies which are signatories to the European cooperation for Accreditation (EA) Multilateral Agreement on Calibration and Testing, or — accredited by the Testing Laboratory Registration Council of New Zealand, or — recognised within the IECEE CB Scheme, or — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement. — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement.or

PROCEDURES FOR DESIGNATING CONFORMITY ASSESSMENT BODIES. The procedures to be followed by New Zealand in designating Conformity Assessment Bodies conformity assessment bodies to assess products against the European Community’s requirements The procedures to be followed by the European Community in designating Conformity Assessment Bodies conformity assessment bodies to assess products against New Zealand’s requirements The Conformity Assessment Bodies conformity assessment bodies listed in Section II will meet the requirements of the Directives listed in Section I, taking into account Council Decision 93/465/EEC of 22 July 1993 concerning the modules for the various phases of the conformity assessment procedures and the rules for the affixing and use of the CE conformity marking, which are intended to be used in the technical harmonisation directives directives, and be are designated on the basis of the procedures defined in the Annex to the Agreement. This may be demonstrated through: (ai) Inspection Product Certification Bodies operating according to the requirements of EN 45004 45011 or ISO Guide 39Guides 28 and 40, and either: 1. The procedures for designating conformity assessment bodies Conformity Assessment Bodies will be consistent with the principles and procedures set out in the Annex to the Agreement. 2. The following procedures are deemed to be consistent with those set out in the Annex to the Agreement: Testing Laboratories(a) Design Verification: For Design Verification, conformity assessment bodies will: — accredited by accreditation bodies which are signatories to the European cooperation for Accreditation (EA) Multilateral Agreement on Calibration and Testingoperate in conformity with EN 45004 or ISO Guide 39, or — accredited by the Testing Laboratory Registration Council of New Zealand, or — recognised within the IECEE CB Scheme, or — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement. — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement.and

PROCEDURES FOR DESIGNATING CONFORMITY ASSESSMENT BODIES. The procedures to be followed by New Zealand Australia in designating Conformity Assessment Bodies conformity assessment bodies to assess products against the European Community’s requirements The procedures to be followed by the European Community in designating Conformity Assessment Bodies conformity assessment bodies to assess products against New ZealandAustralia’s requirements The Conformity Assessment Bodies conformity assessment bodies listed in Section II will meet the requirements of the Directives listed in Section I, taking into account Council Decision 93/465/EEC of 22 July 1993 concerning the modules for the various phases of the conformity assessment procedures and the rules for the affixing and use of the CE conformity marking, which are intended to be used in the technical harmonisation directives and be designated on the basis of the procedures defined in the Annex to the Agreement. This may be demonstrated through: (a) Inspection Product Certification Bodies operating according to the requirements of EN 45004 45011 or ISO Guide 39Guides 28 and 40, and either: 1. The procedures for designating conformity assessment bodies will be consistent with the principles and procedures set out in the Annex to the Agreement. 2. (a) Testing laboratories: The following procedures are deemed to be consistent with those set out in the Annex to the Agreement: Testing Laboratories: — accredited accreditation by an accreditation bodies body which are signatories is a signatory to the European cooperation for Accreditation (EA) Multilateral Agreement on Calibration and Testing, or — accredited by the Testing Laboratory Registration Council of New ZealandXXX-ANZ, or — recognised within the IECEE CB Scheme, or — able ability to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreementunder an equivalent accreditation scheme. — able to demonstrate competence by other means in accordance with Sections A and B of the Annex to the Agreement.