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PART III COMPETENT AUTHORITY FUNCTIONS
27.Grant of approvals by the Northern Ireland competent authority
28.Grant of unilateral and multilateral approvals by the Northern Ireland competent authority in relation to class 7 goods for carriage by rail
29.Appointment of persons by the Northern Ireland competent authority
30.Recognition of approvals, tests, methods, standards and procedures etc. by the Northern Ireland competent authority
31.Imposing of requirements by the Northern Ireland competent authority
32.Issuing of safety adviser vocational training certificates by the Northern Ireland competent authority
33.Issuing of driver training certificates by the Northern Ireland competent authority
35.Miscellaneous functions of the Northern Ireland competent authority
2.Construction of tanks of old tank-vehicles, tank-containers and old tank wagons for carriage by road or rail
3.Testing, examination and maintenance for carriage by road or rail
6.Use of old tank-vehicles, old tank wagons or tank-containers for carriage by road or rail
8.Appointment of inspection bodies by the Northern Ireland competent authority
2.Duties on those designing, manufacturing, importing, supplying, modifying or repairing old pressure receptacles
4.Examination of old pressure receptacles by competent or approved persons
7.Modification, repair and re-rating of old pressure receptacles
8.Additional requirements for old pressure receptacles containing certain dangerous goods not classified as class 2
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 of EC type-examination must be lodged by the...
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 Part IV...
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 components which have been...
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 Part IV...
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...
5.During such visits, the notified body must: ensure that 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.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
4.2.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 item of transportable pressure equipment...
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
4.2.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 item of transportable pressure equipment...
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...
2.The manufacturer must take all measures necessary to ensure that...
3.The notified body must perform the appropriate examinations and tests...
4.Verification by examination and testing of each item of transportable pressure equipment
4.1.Each item of transportable pressure equipment must be individually examined...
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 other member States...
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 equipment which...
4.If the results of the above checks are satisfactory, the...
5.For equipment 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 body or approved body must perform the appropriate...
3.1.All transportable pressure equipment must be examined individually and appropriate...
3.2.The notified body or approved body must affix, or have...
3.3.The owner or his authorised representative established in the Community...
2.The owner or his authorised representative established within the Community...
3.1.The owner or his authorised representative established in the Community...
3.2.Under the quality system, each item of transportable pressure equipment...
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...
PLACARDS, MARKS AND PLATE MARKINGS FOR CARRIAGE WITHIN NORTHERN IRELAND
REASONS FOR EXAMINATION NOT TAKING PLACE OR NOT BEING COMPLETED
1.The applicant for the ADR certificate does not, after being...
2.The particulars relating to the vehicle and shown in any...
5.There is not permanently affixed to the chassis or main...
7.An inspector is not able to complete the inspection without...
10.An inspector is not able to complete the inspection due...
AMENDMENTS TO THE HEALTH AND SAFETY (FEES) REGULATIONS (NORTHERN IRELAND) 2005
1.The Health and Safety (Fees) Regulations (Northern Ireland) 2005 shall...
2.For regulations 11 to 13 there shall be substituted the...
3.For Schedule 8 there shall be substituted the following schedule—...
4.For Schedule 9 there shall be substituted the following schedule—...
5.For Schedule 10 there shall be substituted the following schedule—...
1.Amendments to the Petroleum (Consolidation) Act (Northern Ireland) 1929
2.Amendments to the Dangerous Substances in Harbour Areas Regulations (Northern Ireland) 1991
3.Amendment to the Dangerous Substances (Notification and Marking of Sites) Regulations (Northern Ireland) 1992
4.Amendment to the Notification of New Substances Regulations (Northern Ireland) 1994
5.Amendment to the Health and Safety (Safety Signs and Signals) Regulations (Northern Ireland) 1996
6.Amendments to the Reporting of Injuries, Diseases and Dangerous Occurrences Regulations (Northern Ireland) 1997
7.Amendments to the Radiation (Emergency Preparedness and Public Information) Regulations (Northern Ireland) 2001
8.Amendments to the Control of Asbestos at Work Regulations (Northern Ireland) 2003
9.Amendment to the Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003
10.Amendment to the Control of Lead at Work Regulations (Northern Ireland) 2003
11.Amendment to the Dangerous Substances and Explosive Atmospheres Regulations (Northern Ireland) 2003
12.Amendments to the Pressure Systems Safety Regulations (Northern Ireland) 2004
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