- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/07/2001)
- Gwreiddiol (a wnaed Fel)
There are outstanding changes not yet made by the legislation.gov.uk editorial team to The Transportable Pressure Vessels Regulations 2001. Those changes will be listed when you open the content using the Table of Contents below. Any changes that have already been made by the team appear in the content and are referenced with annotations.
Changes and effects yet to be applied by the editorial team are only applicable when viewing the latest version or prospective version of legislation. They are therefore not accessible when viewing legislation as at a specific point in time. To view the ‘Changes to Legislation’ information for this provision return to the latest version view using the options provided in the ‘What Version’ box above.
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
Final assessment must be performed by the manufacturer and monitored...
During such visits, the notified body must: — ensure that...
Should one or more of the transportable pressure vessels not...
On the responsibility of the notified body, the manufacturer must...
2.The application for EC-type-examination must be lodged by the manufacturer...
A type may cover several versions of the transportable pressure...
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,...
A list of the relevant parts of the technical documentation...
If the notified body refuses to issue an EC type-examination...
6.The applicant must inform the notified body that holds the...
7.Each notified body must communicate to the member States the...
Each notified body must also communicate to the other notified...
9.The manufacturer, or his authorised representative established within the Community,...
Where neither the manufacturer nor his authorised representative is established...
2.The manufacturer, or his authorised representative established within the Community,...
and may cover several versions of the transportable pressure vessel...
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...
A list of the relevant parts of the technical documentation...
If the notified body refuses to issue an EC type-examination...
6.The applicant must inform the notified body that holds the...
7.Each notified body must communicate to the member States the...
Each notified body must also communicate to the other notified...
8.The other notified bodies may on request obtain the relevant...
9.The manufacturer, or his authorised representative established within the Community,...
Where neither the manufacturer nor his authorised representative is established...
2.The manufacturer must take all measures necessary to ensure that...
3.The manufacturer, or his authorised representative established within the Community,...
Where neither the manufacturer nor his authorised representative is established...
4.Final assessment must be subject to monitoring in the form...
During such visits, the notified body must: — ensure that...
Should one or more of the transportable pressure vessels not...
On the responsibility of the notified body, the manufacturer must...
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...
All the elements, requirements and provisions adopted by the manufacturer...
It must contain in particular an adequate description of: —...
3.3.The notified body must assess the quality system to determine...
The decision must be notified to the manufacturer. The notification...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
The manufacturer, or his authorised representative established within the Community,...
The notified body must assess the proposed changes and decide...
It must notify its decision to the manufacturer. The notification...
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...
During such visits the notified body may, if necessary, carry...
6.Each notified body must communicate to the member States the...
Each notified body must also communicate to the other notified...
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...
The application must include: — all relevant information on the...
4.2.The quality system must ensure compliance of the transportable pressure...
All the elements, requirements and provisions adopted by the manufacturer...
It must contain in particular an adequate description of: —...
4.3.The notified body must assess the quality system to determine...
The decision must be notified to the manufacturer. The notification...
4.4.The manufacturer must undertake to fulfil the obligations arising out...
The manufacturer, or his authorised representative established within the Community,...
The notified body must assess the proposed changes and decide...
It must notify its decision to the manufacturer. The notification...
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...
During such visits the notified body may, if necessary, carry...
7.Each notified body must communicate to the member States the...
Each notified body must communicate to the other notified bodies...
2.The manufacturer must operate an approved quality system for production,...
3.1.The manufacturer must lodge an application for assessment of his...
The application must include: — all relevant information on the...
3.2.Under the quality system, each transportable pressure vessel must be...
It must contain in particular an adequate description of: —...
3.3.The notified body must assess the quality system to determine...
The decision must be notified to the manufacturer. The notification...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
The manufacturer, or his authorised representative established within the Community,...
The notified body must assess the proposed changes and decide...
It must notify its decision to the manufacturer. The notification...
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...
During such visits the notified body may, if necessary, carry...
6.Each notified body must communicate to the member States the...
Each notified body must also communicate to the other notified...
2.The manufacturer must draw up the technical documentation described below....
The technical documentation must enable an assessment to be made...
3.The manufacturer must operate an approved quality system for the...
4.1.The manufacturer must lodge an application for assessment of his...
The application must include: — all relevant information on the...
4.2.Under the quality system, each transportable pressure vessel must be...
It must contain in particular an adequate description of: —...
4.3.The notified body must assess the quality system to determine...
The decision must be notified to the manufacturer. The notification...
4.4.The manufacturer must undertake to discharge the obligations arising from...
The manufacturer, or his authorised representative established within the Community,...
The notified body must assess the proposed changes and decide...
It must notify its decision to the manufacturer. The notification...
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...
During such visits the notified body may, if necessary, carry...
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...
The manufacturer, or his authorised representative established within the Community,...
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...
The technical documentation must contain: — a general description of...
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,...
In particular, the notified body must: — examine the technical...
2.The manufacturer must implement an approved quality system for design,...
3.1.The manufacturer must lodge an application for assessment of his...
The application must include: — all relevant information concerning the...
3.2.The quality system must ensure compliance of the transportable pressure...
All the elements, requirements and provisions adopted by the manufacturer...
It must contain in particular an adequate description of: —...
3.3.The notified body must assess the quality system to determine...
The decision must be notified to the manufacturer. The notification...
3.4.The manufacturer must undertake to fulfil the obligations arising out...
The manufacturer, or his authorised representative established within the Community,...
The notified body must assess the proposed changes and decide...
It must notify its decision to the manufacturer. The notification...
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...
During such visits the notified body may, if necessary, carry...
6.Each notified body must communicate to the member States the...
Each notified body must also communicate to the other notified...
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...
The measures carried out must be recorded in documents and...
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...
The measures carried out must be recorded in documents and...
The owner or his authorised representative established within the Community...
The owner or his authorised representative established in the Community...
3.1.The owner or his authorised representative established in the Community...
The application must include: — all relevant information on the...
3.2.Under the quality system, each transportable pressure vessel must be...
It must contain in particular an adequate description of: —...
3.3.The notified body must assess the quality system to determine...
3.4.The owner or his authorised representative established in the Community...
The owner or his authorised representative established in the Community...
The notified body must assess the proposed changes and decide...
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—...
The Whole Instrument you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
The Whole Instrument you have selected contains over 200 provisions and might take some time to download.
Would you like to continue?
Yr Offeryn Cyfan you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Rhestrau you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.
Pwynt Penodol mewn Amser: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys
Mae'r data ar y dudalen hon ar gael yn y fformatau data amgen a restrir: