http://www.legislation.gov.uk/nisr/2003/386/schedule/3/crossheading/this-schedule-substantially-reproduces-the-provisions-of-part-1-of-annex-iv-to-the-transportable-pressure-equipment-directive/paragraph/6n3/madeTransportable Pressure Vessels Regulations (Northern Ireland) 2003Health and safety at workBusiness practice and regulationHealth and safety requirementsMotor industryRegulation and deregulationGovernment Printer for Northern Ireland2016-09-07HEALTH AND SAFETY SCHEDULE 3 CONFORMITY ASSESSMENT PROCEDURES (This Schedule substantially reproduces the provisions of Part 1 of Annex <Acronym Expansion="4">IV</Acronym> to the Transportable Pressure Equipment Directive.)Module D—production quality assurance 6 Each notified body must communicate to the member States the relevant information concerning the quality system approvals which it has withdrawn, and, on request, those it has issued. Each notified body must also communicate to the other notified bodies the relevant information concerning the quality system approvals it has withdrawn or refused.
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<Number>SCHEDULE 3</Number>
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<Title>CONFORMITY ASSESSMENT PROCEDURES</Title>
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(This Schedule substantially reproduces the provisions of Part 1 of Annex
<Acronym Expansion="4">IV</Acronym>
to the Transportable Pressure Equipment Directive.)
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<Title>Module D—production quality assurance</Title>
<P1 DocumentURI="http://www.legislation.gov.uk/nisr/2003/386/schedule/3/crossheading/this-schedule-substantially-reproduces-the-provisions-of-part-1-of-annex-iv-to-the-transportable-pressure-equipment-directive/paragraph/6n3/made" IdURI="http://www.legislation.gov.uk/id/nisr/2003/386/schedule/3/crossheading/this-schedule-substantially-reproduces-the-provisions-of-part-1-of-annex-iv-to-the-transportable-pressure-equipment-directive/paragraph/6n3" id="schedule-3-crossheading-this-schedule-substantially-reproduces-the-provisions-of-part-1-of-annex-iv-to-the-transportable-pressure-equipment-directive_paragraph-6n3" shortId="schedule-3-paragraph-6">
<Pnumber>6</Pnumber>
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<Text>Each notified body must communicate to the member States the relevant information concerning the quality system approvals which it has withdrawn, and, on request, those it has issued.</Text>
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<Text>Each notified body must also communicate to the other notified bodies the relevant information concerning the quality system approvals it has withdrawn or refused.</Text>
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