Chwilio Deddfwriaeth

Chwiliad Uwch

Commission Decision of 21 December 2007 concerning the technical specification of interoperability relating to ‘persons with reduced mobility’ in the trans-European conventional and high-speed rail system (notified under document C(2007) 6633) (Text with EEA relevance) (2008/164/EC) (repealed)

Help about what version

Pa Fersiwn

Rhagor o Adnoddau

PDF o Fersiynau Diwygiedig

Close

Mae hon yn eitem o ddeddfwriaeth sy’n deillio o’r UE

Mae unrhyw newidiadau sydd wedi cael eu gwneud yn barod gan y tîm yn ymddangos yn y cynnwys a chyfeirir atynt gydag anodiadau.Ar ôl y diwrnod ymadael bydd tair fersiwn o’r ddeddfwriaeth yma i’w gwirio at ddibenion gwahanol. Y fersiwn legislation.gov.uk yw’r fersiwn sy’n weithredol yn y Deyrnas Unedig. Y Fersiwn UE sydd ar EUR-lex ar hyn o bryd yw’r fersiwn sy’n weithredol yn yr UE h.y. efallai y bydd arnoch angen y fersiwn hon os byddwch yn gweithredu busnes yn yr UE.

Y fersiwn yn yr archif ar y we yw’r fersiwn swyddogol o’r ddeddfwriaeth fel yr oedd ar y diwrnod ymadael cyn cael ei chyhoeddi ar legislation.gov.uk ac unrhyw newidiadau ac effeithiau a weithredwyd yn y Deyrnas Unedig wedyn. Mae’r archif ar y we hefyd yn cynnwys cyfraith achos a ffurfiau mewn ieithoedd eraill o EUR-Lex.

Changes to legislation:

There are currently no known outstanding effects for the Commission Decision of 21 December 2007 concerning the technical specification of interoperability relating to ‘persons with reduced mobility’ in the trans-European conventional and high-speed rail system (notified under document C(2007) 6633) (Text with EEA relevance) (2008/164/EC) (repealed). Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

  1. Introductory Text

  2. Article 1.. . . . . . . . . ....

  3. Article 2.. . . . . . . . . ....

  4. Article 3.. . . . . . . . . ....

  5. Article 4.. . . . . . . . . ....

  6. Article 5.. . . . . . . . . ....

    1. ANNEX

      TRANS-EUROPEAN CONVENTIONAL AND HIGH-SPEED RAIL SYSTEM

      1. 1. INTRODUCTION

        1. 1.1. Technical scope

        2. 1.2. Geographical scope

        3. 1.3. Content of this TSI

      2. 2. DEFINITION OF SUBSYSTEM/SCOPE

        1. 2.1. Definitions of the subsystems

          1. 2.1.1. Infrastructure

          2. 2.1.2. Rolling Stock

          3. 2.1.3. Telematics Applications for Passengers

        2. 2.2. Definition of ‘persons with reduced mobility’

      3. 3. ESSENTIAL REQUIREMENTS

        1. 3.1. General

        2. 3.2. The essential requirements relate to:

          1. Infrastructure:

          2. Rolling Stock:

        3. 3.3. General requirements

          1. 3.3.1. Safety

          2. 3.3.2. Reliability and availability

          3. 3.3.3. Health

          4. 3.3.4. Environmental protection

          5. 3.3.5. Technical compatibility

        4. 3.4. Requirements specific to the Infrastructure subsystem

          1. 3.4.1. Safety

        5. 3.5. Requirements specific to the Rolling Stock subsystem

          1. 3.5.1. Safety

          2. 3.5.2. Reliability and availability

          3. 3.5.3. Technical compatibility

        6. 3.6. Requirements specific to other subsystems concerning also the Infrastructure and...

          1. 3.6.1. Energy Subsystem

            1. 3.6.1.1. Safety

            2. 3.6.1.2. Environmental protection

            3. 3.6.1.3. Technical compatibility

          2. 3.6.2. Control and command and signalling

            1. 3.6.2.1. Safety

            2. 3.6.2.2. Technical compatibility

          3. 3.6.3. Maintenance

            1. 3.6.3.1. Health and safety

            2. 3.6.3.2. Environmental protection

            3. 3.6.3.3. Technical compatibility

          4. 3.6.4. Operation and traffic management

            1. 3.6.4.1. Safety

            2. 3.6.4.2. Technical compatibility

          5. 3.6.5. Telematics applications for freight and passengers

            1. 3.6.5.1. Technical compatibility

            2. 3.6.5.2. Health

        7. 3.7. Elements of the PRM TSI domain related to the essential...

      4. 4. CHARACTERISATION OF THE SUBSYSTEMS

        1. 4.1. Subsystem Infrastructure

          1. 4.1.1. Introduction

          2. 4.1.2. Functional and technical specifications

            1. 4.1.2.1. General

            2. 4.1.2.2. Parking facilities for PRM

            3. 4.1.2.3. Obstacle-free route

              1. 4.1.2.3.1. General

              2. 4.1.2.3.2. Route identification

            4. 4.1.2.4. Doors and entrances

            5. 4.1.2.5. Floor surfaces

            6. 4.1.2.6. Transparent obstacles

            7. 4.1.2.7. Toilets and baby-changing facilities

              1. 4.1.2.7.1. Subsystem requirements

              2. 4.1.2.7.2. Interoperability constituent requirements

                1. Baby-changing facilities

            8. 4.1.2.8. Furniture and free-standing devices

            9. 4.1.2.9. Ticketing, Information desks and Customer Assistance points

              1. 4.1.2.9.1. Subsystem requirements

              2. 4.1.2.9.2. Interoperability constituent requirements

            10. 4.1.2.10. Lighting

            11. 4.1.2.11. Visual information: signposting, pictograms, dynamic information

              1. 4.1.2.11.1. Subsystem requirements

              2. 4.1.2.11.2. Interoperability constituent requirements

            12. 4.1.2.12. Spoken information

            13. 4.1.2.13. Emergency exits, alarms

            14. 4.1.2.14. Geometry of footbridges and subways

            15. 4.1.2.15. Stairs

            16. 4.1.2.16. Handrails

            17. 4.1.2.17. Ramps, escalators, lifts, travelators

            18. 4.1.2.18. Platform height and offset

              1. 4.1.2.18.1. Platform height

              2. 4.1.2.18.2. Platform offset

              3. 4.1.2.18.3. Track layout along the platforms

            19. 4.1.2.19. Platform width and edge of platform

            20. 4.1.2.20. End of platform

            21. 4.1.2.21. Boarding aids for passengers using wheelchairs

              1. 4.1.2.21.1. Subsystem requirements

                1. Ramps

                2. Platform lifts

              2. 4.1.2.21.2. Interoperability constituent requirements

                1. Ramps

                2. Platform lifts

            22. 4.1.2.22. Level track crossing at stations

          3. 4.1.3. Functional and technical specifications of the interfaces

          4. 4.1.4. Operating rules

          5. 4.1.5. Maintenance rules

          6. 4.1.6. Professional qualifications

          7. 4.1.7. Health and safety conditions

          8. 4.1.8. Infrastructure register

        2. 4.2. Subsystem Rolling Stock

          1. 4.2.1. Introduction

          2. 4.2.2. Functional and technical specifications

            1. 4.2.2.1. General

            2. 4.2.2.2. Seats

              1. 4.2.2.2.1. General

              2. 4.2.2.2.2. Priority seats

                1. 4.2.2.2.2.1. General

                2. 4.2.2.2.2.2. Uni-directional seats

                3. 4.2.2.2.2.3. Facing seats arrangement

            3. 4.2.2.3. Wheelchair spaces

            4. 4.2.2.4. Doors

              1. 4.2.2.4.1. General

              2. 4.2.2.4.2. Exterior doors

                1. 4.2.2.4.2.1. Sub-system requirements

                  1. Passenger door audible warnings — Door enabled for opening

                  2. Passenger door audible warnings — Door close warning

                2. 4.2.2.4.2.2. Interoperability constituent requirements

              3. 4.2.2.4.3. Interior doors

                1. 4.2.2.4.3.1. Sub-system requirements

                2. 4.2.2.4.3.2. Interoperability constituent requirements

            5. 4.2.2.5. Lighting

            6. 4.2.2.6. Toilets

              1. 4.2.2.6.1. General

              2. 4.2.2.6.2. Standard toilet (Interoperability constituent requirements)

              3. 4.2.2.6.3. Universal toilet

                1. 4.2.2.6.3.1. Interoperability constituent requirements (Universal toilet)

                2. 4.2.2.6.3.2. Interoperability constituent requirements (baby change)

            7. 4.2.2.7. Clearways

            8. 4.2.2.8. Customer Information

              1. 4.2.2.8.1. General

              2. 4.2.2.8.2. Information (signage, pictograms inductive loops and emergency call devices)

                1. 4.2.2.8.2.1. Sub-system requirements

                2. 4.2.2.8.2.2. Interoperable constituent requirements

              3. 4.2.2.8.3. Information (route description and seat reservation)

              4. 4.2.2.8.4. Information (Interoperability constituent requirements)

            9. 4.2.2.9. Height changes

            10. 4.2.2.10. Handrails

            11. 4.2.2.11. Wheelchair Accessible sleeping accommodation

            12. 4.2.2.12. Step position for vehicle access and egress

              1. 4.2.2.12.1. General requirements

                1. Requirement a) for all Rolling Stock intended to stop, in...

                2. Requirement b) for all Rolling Stock intended to stop, in...

                3. Requirement c) for all Rolling Stock intended to stop, in...

                4. Requirement d) for all Rolling Stock intended to stop, in...

              2. 4.2.2.12.2. Access/egress steps

              3. 4.2.2.12.3. Boarding aids

                1. 4.2.2.12.3.1. General

                2. 4.2.2.12.3.2. Availability of boarding aids for wheelchair users

                3. 4.2.2.12.3.3. General requirements category A

                  1. Interoperability constituent requirements

                4. 4.2.2.12.3.4. General requirements category B

                  1. Interoperability constituent requirements

                5. 4.2.2.12.3.5. Specific requirements for moveable steps

                6. 4.2.2.12.3.6. Specific requirements for portable ramps

                  1. Interoperability constituent requirements

                  2. Subsystem requirements

                7. 4.2.2.12.3.7. Specific requirements for semi-automatic ramps

                  1. Interoperability constituent requirements

                  2. Subsystem requirements

                8. 4.2.2.12.3.8. Specific requirements for bridging plates

                  1. Interoperability constituent requirements

                9. 4.2.2.12.3.9. Specific requirements for on-board lifts

                  1. Interoperability constituent requirements

                  2. Subsystem requirements

          3. 4.2.3. Functional and technical specifications of the interfaces

          4. 4.2.4. Operating rules

          5. 4.2.5. Maintenance rules

          6. 4.2.6. Professional qualifications

          7. 4.2.7. Health and safety conditions

          8. 4.2.8. Rolling Stock register

        3. 4.3. Definitions of terms used in this TSI

          1. Palm Operated

          2. Contrast

          3. First Step

          4. Slip Resistant

          5. ‘Tactile Signs’ and ‘Tactile Controls’

          6. Station Manager

          7. Safety Information

          8. Safety Instructions

          9. Clearway

          10. Gangway

      5. 5. INTEROPERABILITY CONSTITUENTS

        1. 5.1. Definition

        2. 5.2. Innovative solutions

        3. 5.3. List of constituents

          1. 5.3.1. Infrastructure

          2. 5.3.2. Rolling stock

        4. 5.4. Constituents' performances and specifications

          1. 5.4.1. Infrastructure

          2. 5.4.2. Rolling Stock

      6. 6. ASSESSMENT OF CONFORMITY AND/OR SUITABILITY FOR USE

        1. 6.1. Interoperability constituents

          1. 6.1.1. Conformity assessment (general)

            1. Modules for interoperability constituents:

          2. 6.1.2. Conformity assessment procedures (modules)

          3. 6.1.3. Innovative solutions

          4. 6.1.4. Assessment of suitability for use

        2. 6.2. Subsystems

          1. 6.2.1. Conformity assessment (general)

            1. Modules for the EC verification of subsystems

          2. 6.2.2. Conformity assessment procedures (modules)

          3. 6.2.3. Innovative solutions

          4. 6.2.4. Assessment of maintenance

          5. 6.2.5. Assessment of operational rules

          6. 6.2.6. Assessment of individual vehicles

        3. 6.3. Interoperable Constituents Not Holding an EC Declaration

          1. 6.3.1. General

          2. 6.3.2. The Transition Period

          3. 6.3.3. The Certification of Subsystems Containing Non-Certified Interoperability Constituents during the...

            1. 6.3.3.1. Conditions

            2. 6.3.3.2. Notification

            3. 6.3.3.3. Lifecycle Implementation

          4. 6.3.4. Monitoring Arrangements

      7. 7. IMPLEMENTATION OF THE PRM TSI

        1. 7.1. Application of this TSI to new Infrastructure/Rolling Stock

          1. 7.1.1. Infrastructure

          2. 7.1.2. Rolling Stock

            1. 7.1.2.1. General

            2. 7.1.2.2. Newly built Rolling Stock of new design

              1. 7.1.2.2.1. Definitions

              2. 7.1.2.2.2. General

              3. 7.1.2.2.3. Phase A

              4. 7.1.2.2.4. Phase B

            3. 7.1.2.3. Rolling Stock of an existing design

            4. 7.1.2.4. Transitional Period

        2. 7.2. TSI Revision

        3. 7.3. Application of this TSI to existing Infrastructure/Rolling Stock

          1. 7.3.1. Infrastructure

            1. 7.3.1.1. General

            2. 7.3.1.2. Obstacles-free routes — General (4.1.2.4.1)

            3. 7.3.1.3. Geometry of footbridges, stairways and subways (4.1.2.14 and 4.1.2.15)

            4. 7.3.1.4. Ramps, escalators, lifts and travelators (4.1.2.17)

            5. 7.3.1.5. Platform width and edge of platform (4.1.2.19)

            6. 7.3.1.6. Platform height and offset (4.1.2.18)

            7. 7.3.1.7. Buildings of an historic nature

          2. 7.3.2. Rolling Stock

            1. 7.3.2.1. General

            2. 7.3.2.2. Seats

            3. 7.3.2.3. Wheelchair Spaces

            4. 7.3.2.4. Exterior doors

            5. 7.3.2.5. Interior doors

            6. 7.3.2.6. Lighting

            7. 7.3.2.7. Toilets

            8. 7.3.2.8. Clearways

            9. 7.3.2.9. Information

            10. 7.3.2.10. Height Changes

            11. 7.3.2.11. Handrails

            12. 7.3.2.12. Wheelchair Accessible sleeping accommodation

            13. 7.3.2.13. Step positions, steps and boarding aids

        4. 7.4. Specific cases

          1. 7.4.1. General

            1. 7.4.1.1. Platform height

            2. 7.4.1.2. Platform offset

            3. 7.4.1.3. Access and egress steps

              1. 7.4.1.3.1. General

              2. 7.4.1.3.2. Specific case for Rolling Stock operating in Great Britain ‘P’...

              3. 7.4.1.3.3. Specific case for Rolling Stock operating in Finland ‘P’

              4. 7.4.1.3.4. Specific case for Rolling Stock intending to operate on the...

            4. 7.4.1.4. Clearways

            5. 7.4.1.5. Audible Door Signals according to chapter 4.2.2.4.1 ‘P’

            6. 7.4.1.6. Priority Seats ‘P’

            7. 7.4.1.7. Obstacle free routes ‘P’ (Clause 4.1.2.3.1)

            8. 7.4.1.8. Passenger Numbers

        5. 7.5. Rolling Stock operating under national, bilateral, multilateral or international agreements...

          1. 7.5.1. Existing agreements

          2. 7.5.2. Future agreements

        6. 7.6. Placing in service of Infrastructure and Rolling Stock

    2. ANNEXES (TO THE TSI)

      Scope: Whole Subsystems Aspect: Accessibility for Persons with Reduced Mobility

      1. . . . . . . . . . ....

      2. ANNEX A

        1. . . . . . . . . . ....

      3. ANNEX B

        1. . . . . . . . . . ....

      4. ANNEX C

        Assessment of Maintenance Arrangements: Conformity Assessment Procedure (Annex F4)

        1. . . . . . . . . . ....

      5. ANNEX D

        Assessment of interoperability constituents

        1. D.1 Scope

        2. D.2 Characteristics

      6. ANNEX E

        Assessment of the subsystems

        1. E.1 Scope

        2. E.2 Characteristics and modules

      7. ANNEX F

        Procedures for assessment of conformity and suitability for use

        1. F.1. List of the modules

        2. F.2. Modules for Interoperability Constituents

          1. F.2.1. Module A: Internal production control

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. The technical documentation shall enable the conformity of the interoperability...

            4. 4. . . . . . . . . . ....

            5. 5. The manufacturer or his authorised representative established within the Community...

            6. 6. The manufacturer or his authorised representative shall keep a copy...

            7. 7. . . . . . . . . . ....

          2. F.2.2. Module A1: Internal Design Control with Production Verification

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. The technical documentation shall enable the conformity of the interoperability...

            4. 4. . . . . . . . . . ....

            5. 5. . . . . . . . . . ....

            6. 5.1. Verification by examination and testing of every product

              1. 5.1.1. . . . . . . . . . ....

              2. 5.1.2. . . . . . . . . . ....

            7. 5.2. Statistical verification

              1. 5.2.1. . . . . . . . . . ....

              2. 5.2.2. . . . . . . . . . ....

              3. 5.2.3. . . . . . . . . . ....

              4. 5.2.4. . . . . . . . . . ....

              5. 5.2.5. . . . . . . . . . ....

            8. 6. The manufacturer or his authorised representative established within the Community...

            9. 7. The manufacturer or his authorised representative shall keep a copy...

            10. 8. . . . . . . . . . ....

          3. F.2.3. Module B: Type Examination

            1. 1. . . . . . . . . . ....

            2. 2. The application for the EC type-examination shall be lodged by...

            3. 3. The technical documentation shall enable the conformity of the interoperability...

            4. 4. . . . . . . . . . ....

            5. 4.1. . . . . . . . . . ....

            6. 4.2. . . . . . . . . . ....

            7. 4.3. . . . . . . . . . ....

            8. 4.4. . . . . . . . . . ....

            9. 4.5. . . . . . . . . . ....

            10. 4.6. . . . . . . . . . ....

            11. 4.7. . . . . . . . . . ....

            12. 4.8. . . . . . . . . . ....

            13. 5. Where the type meets the provisions of the TSI, the...

            14. 6. . . . . . . . . . ....

            15. 7. . . . . . . . . . ....

            16. 8. . . . . . . . . . ....

            17. 9. . . . . . . . . . ....

            18. 10. . . . . . . . . . ....

          4. F.2.4. Module C: Conformity to Type

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. The manufacturer or his authorised representative established within the Community...

            4. 4. The manufacturer or his authorised representative established within the Community...

            5. 5. . . . . . . . . . ....

          5. F.2.5. Module D: Production Quality Management System

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. . . . . . . . . . ....

            4. 3.1. The manufacturer shall lodge an application for assessment of his...

            5. 3.2. The quality management system shall ensure compliance of the interoperability...

            6. 3.3. The notified body assesses the quality management system to determine...

            7. 3.4. The manufacturer shall undertake to fulfil the obligations arising out...

            8. 4. . . . . . . . . . ....

            9. 4.1. . . . . . . . . . ....

            10. 4.2. The manufacturer shall allow the notified body entrance for inspection...

            11. 4.3. The notified body shall periodically carry out audits to make...

            12. 4.4. . . . . . . . . . ....

            13. 5. Each notified body shall communicate to the other notified bodies...

            14. 6. The manufacturer shall, for a period of 10 years after...

            15. 7. The manufacturer or his authorised representative established within the Community...

            16. 8. The manufacturer or his authorised representative established within the Community...

            17. 9. . . . . . . . . . ....

          6. F.2.6. Module F: Product Verification

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. . . . . . . . . . ....

            4. 4. Verification by examination and testing of every interoperability constituent

              1. 4.1. . . . . . . . . . ....

              2. 4.2. . . . . . . . . . ....

              3. 4.3. . . . . . . . . . ....

            5. 5. Statistical verification

              1. 5.1. . . . . . . . . . ....

              2. 5.2. . . . . . . . . . ....

              3. 5.3. . . . . . . . . . ....

              4. 5.4. In the case of accepted lots, the notified body shall...

              5. 5.5. . . . . . . . . . ....

            6. 6. The manufacturer or his authorised representative established within the Community...

            7. 7. The manufacturer or his authorised representative established within the Community...

            8. 8. . . . . . . . . . ....

          7. F.2.7. Module H1: Full Quality Management System

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. Quality management system

              1. 3.1. The manufacturer shall lodge an application for assessment of his...

              2. 3.2. The quality management system shall ensure compliance of the interoperability...

              3. 3.3. The notified body shall assess the quality management system to...

              4. 3.4. The manufacturer shall undertake to fulfil the obligations arising out...

            4. 4. . . . . . . . . . ....

            5. 4.1. . . . . . . . . . ....

            6. 4.2. The manufacturer shall allow the notified body entrance for inspection...

            7. 4.3. The notified body shall periodically carry out audits to make...

            8. 4.4. . . . . . . . . . ....

            9. 5. The manufacturer shall, for a period of 10 years after...

            10. 6. Each notified body shall communicate to the other notified bodies...

            11. 7. The manufacturer or its authorised representative established within the Community...

            12. 8. The manufacturer or his authorised representative established within the Community...

            13. 9. . . . . . . . . . ....

          8. F.2.8. Module H2: Full Quality Management System With Design Examination

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

            3. 3. Quality management system

              1. 3.1. The manufacturer shall lodge an application for assessment of his...

              2. 3.2. The quality management system shall ensure compliance of the interoperability...

              3. 3.3. The notified body shall assess the quality management system to...

              4. 3.4. The manufacturer shall undertake to fulfil the obligations arising out...

            4. 4. . . . . . . . . . ....

            5. 4.1. . . . . . . . . . ....

            6. 4.2. The manufacturer shall allow the notified body entrance for inspection...

            7. 4.3. The notified body shall periodically carry out audits to make...

            8. 4.4. . . . . . . . . . ....

            9. 5. The manufacturer shall, for a period of 10 years after...

            10. 6. Design examination

              1. 6.1. . . . . . . . . . ....

              2. 6.2. The application shall enable the design, manufacture, maintenance and operation...

              3. 6.3. . . . . . . . . . ....

              4. 6.4. The notified body shall examine the application and assess the...

              5. 6.5. . . . . . . . . . ....

              6. 6.6. . . . . . . . . . ....

            11. 7. Each notified body shall communicate to the other notified bodies...

            12. 8. The manufacturer or his authorised representative established within the Community...

            13. 9. The manufacturer or his authorised representative established within the Community...

            14. 10. . . . . . . . . . ....

          9. F.2.9. Module V: Type-Validation By In Service Experience (Suitability For Use)...

            1. 1. . . . . . . . . . ....

            2. 2. The manufacturer, or his authorised representative established within the Community,...

            3. 3. The technical documentation shall enable the assessment of the product...

            4. 4. The programme for the validation by in service experience shall...

            5. 5. . . . . . . . . . ....

            6. 5.1. . . . . . . . . . ....

            7. 5.2. . . . . . . . . . ....

            8. 5.3. . . . . . . . . . ....

            9. 5.4. . . . . . . . . . ....

            10. 5.5. . . . . . . . . . ....

            11. 5.6. . . . . . . . . . ....

            12. 5.7. . . . . . . . . . ....

            13. 6. Where the type meets the provisions of the TSI, the...

            14. 7. . . . . . . . . . ....

            15. 8. . . . . . . . . . ....

            16. 9. . . . . . . . . . ....

            17. 10. . . . . . . . . . ....

            18. 11. The manufacturer or his authorised representative established within the Community...

            19. 12. The manufacturer or his authorised representative established within the Community...

        3. F.3. Modules for the EC Verification of Subsystems

          1. F.3.1. Module SB: Type Examination

            1. 1. This module describes the EC verification procedure whereby a notified...

            2. 2. The contracting entity shall lodge an application for EC verification...

            3. 3. The applicant shall place at the disposal of the notified...

            4. 4. . . . . . . . . . ....

            5. 4.1. . . . . . . . . . ....

            6. 4.2. . . . . . . . . . ....

            7. 4.3. . . . . . . . . . ....

            8. 4.4. . . . . . . . . . ....

            9. 4.5. . . . . . . . . . ....

            10. 4.6. . . . . . . . . . ....

            11. 4.7. . . . . . . . . . ....

            12. 5. Where the type meets the provisions of the TSI, the...

            13. 6. . . . . . . . . . ....

            14. 7. . . . . . . . . . ....

            15. 8. . . . . . . . . . ....

            16. 9. . . . . . . . . . ....

          2. F.3.2. Module SD: Production Quality Management System

            1. 1. This module describes the EC verification procedure whereby a notified...

            2. 2. The notified body carries out the procedure, under the condition,...

            3. 3. For the subsystem that is subject of the EC verification...

            4. 4. EC verification procedure

              1. 4.1. The contracting entity shall lodge an application for EC verification...

              2. 4.2. The application shall include:

              3. 4.3. The notified body shall fist examine the application concerning the...

            5. 5. Quality management system

              1. 5.1. The contracting entity, if involved, and the main contractor, when...

              2. 5.2. For the contracting entity or the main contractor responsible for...

              3. 5.3. The notified body chosen by the contracting entity shall examine,...

              4. 5.4. The notified body referenced to in point 5.1. shall assess...

              5. 5.5. The contracting entity, if involved, and the main contractor shall...

            6. 6. . . . . . . . . . ....

            7. 6.1. . . . . . . . . . ....

            8. 6.2. The contracting entity, if involved, and the main contractor shall...

            9. 6.3. The notified body shall periodically carry out audits to make...

            10. 6.4. . . . . . . . . . ....

            11. 6.5. The notified body chosen by the contracting entity and responsible...

            12. 7. . . . . . . . . . ....

            13. 8. The contracting entity, if involved, and the main contractor shall,...

            14. 9. Where the subsystem meets the requirements of the TSI, the...

            15. 10. The notified body chosen by the contracting entity shall be...

            16. 11. Each notified body shall communicate to the other notified bodies...

            17. 12. The records accompanying the certificate of conformity shall be lodged...

          3. F.3.3. Module SF: Product Verification

            1. 1. This module describes the EC verification procedure whereby a notified...

            2. 2. The contracting entity shall lodge an application for EC verification...

            3. 3. Within that part of the procedure the contracting entity checks...

            4. 4. . . . . . . . . . ....

            5. 5. The application shall enable the design, manufacture, installation, maintenance and...

            6. 6. The notified body shall first examine the application concerning the...

            7. 7. . . . . . . . . . ....

            8. 7.1. . . . . . . . . . ....

            9. 7.2. . . . . . . . . . ....

            10. 8. The notified body shall agree with the contracting entity (and...

            11. 9. Where the subsystem meets the requirements of the TSI, the...

            12. 10. The notified body shall be responsible for compiling the technical...

            13. 11. The records accompanying the certificate of conformity shall be lodged...

          4. F.3.4. Module SG: Unit verification

            1. 1. This module describes the EC verification procedure whereby a notified...

            2. 2. The contracting entity shall lodge an application for EC verification...

            3. 3. The technical documentation shall enable the design, manufacture, installation and...

            4. 4. The notified body shall examine the application and the technical...

            5. 5. . . . . . . . . . ....

            6. 6. . . . . . . . . . ....

            7. 7. Where the subsystem meets the requirements of the TSI, the...

            8. 8. The notified body shall be responsible for compiling the technical...

            9. 9. The records accompanying the certificate of conformity shall be lodged...

          5. F.3.5. Module SH2: Full Quality Management System with Design Examination

            1. 1. This module describes the EC verification procedure whereby a notified...

            2. 2. The notified body shall carry out the procedure, including a...

            3. 3. For the subsystem that is subject of the EC verification...

            4. 4. EC verification procedure

              1. 4.1. . . . . . . . . . ....

              2. 4.2. The application shall enable the design, manufacture, assembly, installation, maintenance...

              3. 4.3. . . . . . . . . . ....

              4. 4.4. The notified body shall examine the application concerning the design...

              5. 4.5. . . . . . . . . . ....

            5. 5. Quality management system

              1. 5.1. The contracting entity, if involved, and the main contractor, when...

              2. 5.2. For the contracting entity or the main contractor responsible for...

              3. 5.3. The notified body chosen by the contracting entity shall examine,...

              4. 5.4. The notified body referenced in point 5.1. shall assess the...

              5. 5.5. The contracting entity, if involved, and the main contractor shall...

            6. 6. . . . . . . . . . ....

            7. 6.1. . . . . . . . . . ....

            8. 6.2. The contracting entity, if involved, and the main contractor shall...

            9. 6.3. The notified body shall periodically carry out audits to make...

            10. 6.4. . . . . . . . . . ....

            11. 6.5. The notified body chosen by the contracting entity and responsible...

            12. 7. . . . . . . . . . ....

            13. 8. The contracting entity, if involved, and the main contractor shall,...

            14. 9. Where the subsystem meets the requirements of the TSI, the...

            15. 10. The notified body chosen by the contracting entity shall be...

            16. 11. Each notified body shall communicate to the other notified bodies...

            17. 12. The records accompanying the certificate of conformity shall be lodged...

        4. F.4. Assessment of Maintenance Arrangements: Conformity Assessment Procedure

      8. ANNEX G

        1. . . . . . . . . . ....

      9. ANNEX H

        1. . . . . . . . . . ....

      10. ANNEX I

        1. . . . . . . . . . ....

      11. ANNEX J

        1. . . . . . . . . . ....

      12. ANNEX K

        1. . . . . . . . . . ....

      13. ANNEX L

        Aspects not specified in the PRM TSI and for which European Rules apply or notification of National Rules is required

      14. ANNEX M

        Transportable Wheelchair

        1. M.1 Scope

        2. M.2 Characteristics

      15. ANNEX N

        PRM Signage

        1. N.1 Scope

        2. N.2 Infrastructure signs

        3. N.3 Rolling stock signs

        4. N.4 International wheelchair sign

        5. N.5 Inductive loop sign

        6. N.6 Call for assistance/call for information sign

        7. N.7 Emergency call sign

        8. N.8 Priority seating signs

Yn ôl i’r brig

Options/Help

Print Options

You have chosen to open the Whole Decision

The Whole Decision 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?

You have chosen to open Schedules only

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?

Close

Mae deddfwriaeth ar gael mewn fersiynau gwahanol:

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 mabwysiadwyd gan yr UE): Mae'r wreiddiol version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.

Close

Dewisiadau Agor

Dewisiadau gwahanol i agor deddfwriaeth er mwyn gweld rhagor o gynnwys ar y sgrin ar yr un pryd

Close

Rhagor o Adnoddau

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:

  • y PDF print gwreiddiol y fel adopted version that was used for the EU Official Journal
  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • pob fformat o’r holl ddogfennau cysylltiedig
  • slipiau cywiro
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill
Close

Llinell Amser Newidiadau

Mae’r llinell amser yma yn dangos y fersiynau gwahanol a gymerwyd o EUR-Lex yn ogystal ag unrhyw fersiynau dilynol a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig.

Cymerir dyddiadau fersiynau’r UE o ddyddiadau’r dogfennau ar EUR-Lex ac efallai na fyddant yn cyfateb â’r adeg pan ddaeth y newidiadau i rym ar gyfer y ddogfen.

Ar gyfer unrhyw fersiynau a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig, bydd y dyddiad yn cyd-fynd â’r dyddiad cynharaf y daeth y newid (e.e. ychwanegiad, diddymiad neu gyfnewidiad) a weithredwyd i rym. Am ragor o wybodaeth gweler ein canllaw i ddeddfwriaeth ddiwygiedig ar Ddeall Deddfwriaeth.

Close

Rhagor o Adnoddau

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:

  • y PDF print gwreiddiol y fel adopted fersiwn a ddefnyddiwyd am y copi print
  • slipiau cywiro

liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys

  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill