CONFORMITY ASSESSMENT PROCEDURES
2.The manufacturer must draw up the technical documentation described in...
3.The technical documentation must enable an assessment to be made...
4.The manufacturer, or his authorised representative established within the Community,...
5.The manufacturer must take all measures necessary to ensure that...
Module A1—internal manufacturing checks with monitoring of the final assessment
2.The application for EC-type-examination must be lodged by the manufacturer...
3.The technical documentation must enable an assessment to be made...
4.1.examine the technical documentation, verify that the type has been...
4.2.perform or have performed the appropriate examinations and necessary tests...
4.3.perform or have performed the appropriate examinations and necessary tests...
4.4.agree with the applicant the location where the examinations and...
5.Where the type satisfies the relevant provisions of these Regulations,...
6.The applicant must inform the notified body that holds the...
7.Each notified body must communicate to the member States the...
9.The manufacturer, or his authorised representative established within the Community,...
2.The manufacturer, or his authorised representative established within the Community,...
3.The technical documentation must enable an assessment to be made...
4.1.examine the technical documentation and identify the components which have...
4.2.perform the necessary examinations to establish whether the solutions adopted...
4.3.perform the necessary examinations to establish whether the relevant provisions...
5.Where the design meets the relevant provisions of these Regulations...
6.The applicant must inform the notified body that holds the...
7.Each notified body must communicate to the member States the...
8.The other notified bodies may on request obtain the relevant...
9.The manufacturer, or his authorised representative established within the Community,...
2.The manufacturer must take all measures necessary to ensure that...
3.The manufacturer, or his authorised representative established within the Community,...
4.Final assessment must be subject to monitoring in the form...
2.The manufacturer must operate an approved quality system for production,...
3.1.The manufacturer must lodge an application for assessment of his...
3.2.The quality system must ensure compliance of the transportable pressure...
3.3.The notified body must assess the quality system to determine...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
4.Surveillance under the responsibility of the notified body
4.1.The purpose of surveillance is to ensure that the manufacturer...
4.2.The manufacturer must allow the notified body access for inspection...
4.3.The notified body must carry out periodic audits to make...
4.4.In addition, the notified body may pay unexpected visits to...
6.Each notified body must communicate to the member States the...
2.The manufacturer must draw up the technical documentation described below....
3.The manufacturer must operate an approved quality system for production,...
4.1.The manufacturer must lodge an application for assessment of his...
4.2.The quality system must ensure compliance of the transportable pressure...
4.3.The notified body must assess the quality system to determine...
4.4.The manufacturer must undertake to fulfil the obligations arising out...
5.Surveillance under the responsibility of the notified body
5.2.The manufacturer must allow the notified body access for inspection...
5.3.The notified body must carry out periodic audits to make...
5.4.In addition, the notified body may pay unexpected visits to...
7.Each notified body must communicate to the member States the...
2.The manufacturer must operate an approved quality system for production,...
3.1.The manufacturer must lodge an application for assessment of his...
3.2.Under the quality system, each transportable pressure vessel must be...
3.3.The notified body must assess the quality system to determine...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
4.Surveillance under the responsibility of the notified body
4.1.The purpose of surveillance is to ensure that the manufacturer...
4.2.The manufacturer must allow the notified body access for inspection...
4.3.The notified body must carry out periodic audits to make...
4.4.In addition, the notified body may pay unexpected visits to...
6.Each notified body must communicate to the member States the...
2.The manufacturer must draw up the technical documentation described below....
3.The manufacturer must operate an approved quality system for the...
4.1.The manufacturer must lodge an application for assessment of his...
4.2.Under the quality system, each transportable pressure vessel must be...
4.3.The notified body must assess the quality system to determine...
4.4.The manufacturer must undertake to discharge the obligations arising from...
5.Surveillance under the responsibility of the notified body
5.2.The manufacturer must allow the notified body access for inspection...
5.3.The notified body must carry out periodic audits to make...
5.4.In addition, the notified body may pay unexpected visits to...
7.Each notified body must communicate to the member States the...
Each notified body must communicate to the other notified bodies the relevant information concerning the quality system approvals it has withdrawn or refused.
2.The manufacturer must take all measures necessary to ensure that...
The manufacturer, or his authorised representative established within the Community, must affix the conformity marking to all transportable pressure vessels and draw up a declaration of conformity.
3.The notified body must perform the appropriate examinations and tests...
4.Verification by examination and testing of each transportable pressure vessel
4.1.Each transportable pressure vessel must be individually examined and must...
4.2.The notified body must affix its identification number or have...
4.3.The manufacturer, or his authorised representative established within the Community,...
3.The technical documentation must enable the conformity of the transportable...
4.The notified body must examine the design and construction of...
4.1.The notified body must affix its identification number or have...
4.2.The manufacturer, or his authorised representative established within the Community,...
2.The manufacturer must implement an approved quality system for design,...
3.1.The manufacturer must lodge an application for assessment of his...
3.2.The quality system must ensure compliance of the transportable pressure...
3.3.The notified body must assess the quality system to determine...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
4.Surveillance under the responsibility of the notified body
4.1.The purpose of this surveillance is to make sure that...
4.2.The manufacturer must allow the notified body access for inspection...
4.3.The notified body must carry out periodic audits to make...
4.4.In addition, the notified body may pay unexpected visits to...
6.Each notified body must communicate to the member States the...
1.Module H1—full quality assurance with design examination and special surveillance of the final test
2.Final assessment is subject to increased surveillance in the form...
CONFORMITY REASSESSMENT PROCEDURE
1.This procedure describes the method for ensuring that transportable pressure...
2.The owner must make available to a notified body information...
3.The notified body must check whether transportable pressure vessels which...
4.If the results of the above checks are satisfactory, the...
5.For vessels manufactured in series, including their valves and other...
PERIODIC INSPECTION PROCEDURES
2.To meet the requirements referred to in paragraph 1, the...
3.The notified or approved body must perform the appropriate examinations...
3.1.All transportable pressure vessels must be examined individually and appropriate...
3.2.The notified or approved body must affix, or have affixed,...
3.3.The owner or his authorised representative established in the Community...
2.The owner or his authorised representative established in the Community...
3.1.The owner or his authorised representative established in the Community...
3.2.Under the quality system, each transportable pressure vessel must be...
3.3.The notified body must assess the quality system to determine...
3.4.The owner or his authorised representative established in the Community...
4.Surveillance under the responsibility of the notified body
4.2.The owner or his authorised representative established in the Community...
4.3.The notified body must carry out periodic audits to make...
4.4.In addition, the notified body may pay unannounced visits to...
5.The owner or his authorised representative established in the Community...
AMENDMENTS TO THE CDGCPL REGULATIONS
1.The CDGCPL Regulations shall be amended in accordance with the...
3.In regulation 2(1)— (a) for the definition of “competent person”...
4.For paragraphs (4) and (5) of regulation 3, there shall...
6.In regulation 19, for paragraph (5) there shall be substituted...
10.For Schedule 8 there shall be substituted the following Schedule—...