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Article 1.The TSI relating to the ‘rolling stock’ subsystem of the...
Article 2.(1) With regard to the aspects that are common to...
Article 3.(1) For the purposes of this Article: ‘upgrading’ means major...
Article 4.The relevant parts of Commission recommendation 2001/290/EC on the basic...
Article 5.The attached TSI shall enter into force six months after...
Technical specification for interoperability relating to the rolling stock subsystem
4. CHARACTERISTICS OF THE SUBSYSTEM
4.1. BASIC PARAMETERS OF THE ROLLING STOCK SUBSYSTEM
4.1.6. Electrical boundary characteristics for rolling stock (BP14)
4.1.7. Mechanical boundary characteristics for rolling stock (BP15)
4.1.8. Boundary characteristics linked to exterior noise (BP17)
4.1.9. Boundary Characteristics linked to exterior electromagnetic interference (BP19)
4.1.10. Boundary characteristics linked to interior noise (BP20)
4.1.11. Boundary characteristics linked to air conditioning (BP21)
4.1.12. Characteristics linked to the carriage of persons of reduced mobility...
4.2. ROLLING STOCK SUBSYSTEM INTERFACES
5. INTEROPERABILITY CONSTITUENTS
5.1. According to Article 2(d) of Directive 96/48/EC the interoperability constituents...
5.2. The interoperability constituents are subject to the relevant provisions of...
5.3. These interoperability constituents are subject to performance specifications Assessment of...
5.4. For the purposes of this TSI the following are declared...
6. ASSESSMENT OF CONFORMITY AND/OR SUITABILITY FOR USE
PROCEDURES FOR ASSESSMENT OF CONFORMITY AND SUITABILITY FOR USE
MODULE A (INTERNAL PRODUCTION CONTROL) Conformity assessment of interoperability constituents
1. This module describes the procedure whereby the manufacturer or his...
2. The manufacturer must prepare the technical documentation described in point...
3. The technical documentation must enable the conformity of the interoperability...
4. The manufacturer must take all the measures necessary in order...
5. The manufacturer or his authorised representative established within the Community...
6. The manufacturer or his authorised representative must keep a copy...
7. If in addition to the EC declaration of conformity, an...
MODULE B (TYPE-EXAMINATION) Conformity assessment of interoperability constituents
1. This module describes that part of the procedure by which...
3. The technical documentation must enable the conformity of the interoperability...
4.3. if a review of the manufacturing process is requested in...
4.5. identify the elements which have been designed in accordance with...
4.6. perform or have performed the appropriate examinations and necessary tests...
4.7. perform or have performed the appropriate examinations and necessary tests...
4.8. agree with the applicant the location where the examinations and...
6. The applicant must inform the notified body that holds the...
8. Each notified body must communicate to the other notified bodies...
9. The other notified bodies will receive copies of the type-examination...
10. The manufacturer or his authorised representative established within the Community...
MODULE D (PRODUCTION QUALITY ASSURANCE) Conformity assessment of interoperability constituents
1. This module describes the procedure whereby the manufacturer or his...
2. The manufacturer must operate an approved quality system for production,...
3.1. 3.1.The manufacturer must lodge an application for assessment of his...
3.2. The quality system must ensure compliance of the interoperability constituents...
3.3. The notified body must assess the quality system to determine...
3.4. The manufacturer must undertake to fulfil the obligations arising out...
3.5. Each notified body must communicate to the other notified bodies...
3.6. The other notified bodies will receive copies of the quality...
4. Surveillance of the quality system under the responsibility of the...
6. The manufacturer or his authorised representative established within the Community...
7. The manufacturer or his authorised representative established within the Community...
8. If additional to the EC declaration of conformity an EC...
MODULE F (PRODUCT VERIFICATION) Conformity assessment of interoperability constituents
1. This module describes that part of the procedure whereby a...
2. The manufacturer must take all measures necessary in order that...
3. The notified body must carry out the appropriate examinations and...
4. Verification by examination and testing of every interoperability constituent
5.1. The manufacturer must present his interoperability constituents in the form...
5.2. All interoperability constituents must be available for verification in the...
5.3. The statistical procedure must use appropriate elements (statistical method, sampling...
5.4. In the case of accepted lots, the notified body shall...
5.5. The manufacturer or his authorised representative established within the Community...
6. The manufacturer or his authorised representative established within the Community...
7. The manufacturer or his authorised representative established within the Community...
8. If additional to the EC declaration of conformity an EC...
1. This module describes the procedure whereby a notified body carries...
2. The manufacturer must operate 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 interoperability constituent...
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 of the quality system under the responsibility of the...
6.1. The manufacturer must lodge an application for examination of the...
6.2. The application must enable the design, manufacture and operation of...
6.3. The notified body must examine the application and where the...
6.4. The applicant must keep the notified body that has issued...
6.5. If no modifications as under point 6.4 have been made...
7. Each notified body must communicate to the other notified bodies...
8. The manufacturer or his authorised representative established within the Community...
9. The manufacturer, or his authorised representative established within the Community,...
10. If additional to the EC declaration of conformity an EC...
1. This module describes that part of the procedure by which...
2. The application for the type-validation by in service experience must...
3. The technical documentation must enable the assessment of the product...
4. The programme for the validation by in service experience must...
5.1. examine the technical documentation and the programme for validation by...
5.2. verify that the type is representative and has been manufactured...
5.3. verify that the programme for validation by in-service experience is...
5.4. agree with the applicant about the programme and the location...
5.5. monitor and inspect the progress of in service running, operation...
5.6. evaluate the report, to be issued by the company (infrastructure...
5.7. assess, if the in-service behaviour meets the requirements of Directive...
7. The applicant must inform the notified body that holds the...
9. Each notified body must communicate to the other notified bodies...
10. The other notified bodies will receive copies of the suitability...
11. The manufacturer or his authorised representative established within the Community...
12. The manufacturer or his authorised representative established within the Community...
13. The manufacturer or his authorised representative established within the Community...
MODULE SB (EC TYPE-EXAMINATION) EC verification of rolling stock subsystem
1. This module describes part of the EC verification procedure whereby...
2. The adjudicating entity or its authorised representative established within the...
3. The applicant must place at the disposal of the notified...
4.4. identify the elements which have been designed in accordance with...
4.5. perform or have performed the appropriate examinations and necessary tests...
4.6. perform or have performed the appropriate examinations and necessary tests...
4.7. agree with the applicant the location where the examinations and...
5. Where the type meets the provisions of Directive 96/48 /EC...
6. The applicant must inform the notified body that holds the...
8. Each notified body must communicate to the other notified bodies...
9. The other notified bodies will receive copies of the type-examination...
10. The adjudicating entity or its authorised representative established within the...
MODULE SD (PRODUCTION QUALITY ASSURANCE) EC verification of rolling stock subsystem
1. This module describes the EC verification procedure whereby a notified...
4. Surveillance of the quality system(s) under the responsibility of the...
4.1. The purpose of surveillance is to make sure that the...
4.2. The notified body as referred to under point 3.1 must...
4.3. The manufacturer(s) and, if involved, the adjudicating entity or its...
4.4. The notified body(ies) must periodically carry out audits to make...
4.5. Additionally the notified body(ies) may pay unexpected visits to the...
5. The manufacturer(s) and, if involved the adjudicating entity must, for...
6.1. The adjudicating entity or its authorised representative established within the...
6.2. The application must enable the design, manufacture, assembling, installation and...
6.3. The notified body must examine the application concerning the validity...
6.4. The notified body must then examine if the approval and...
6.5. The notified body responsible for the EC verification, if not...
6.6. Where the subsystem meets the requirements of the TSI, the...
6.7. The notified body shall be responsible for compiling the technical...
7. The complete records accompanying the certificate of EC verification must...
8. The adjudicating entity or its authorised representative within the Community...
MODULE SF (PRODUCT VERIFICATION) EC verification of a rolling stock subsystem
1. This module describes the EC verification procedure whereby a notified...
2. The adjudicating entity or its authorised representative established within the...
3. Within that part of the procedure the adjudicating entity or...
4. The adjudicating entity must take all measures necessary in order...
5. The technical documentation must enable the design, manufacture, installation and...
6. The notified body must carry out the appropriate examinations and...
7. Verification by examination and testing of every subsystem (as a...
8. The notified body may agree with the adjudicating entity the...
9. The notified body must have permanent access for testing and...
10. Where the subsystem meets the requirements of the Directive 96/48/EC...
11. The notified body shall be responsible for compiling the technical...
12. The complete records accompanying the certificate of EC verification must...
13. The adjudicating entity or its authorised representative within the Community...
1. This module describes the EC verification procedure whereby a notified...
2. For the subsystem, subject of the EC verification procedure, the...
4. Surveillance of the quality system(s) under the responsibility of the...
4.1. The purpose of surveillance is to make sure that the...
4.2. The notified body(ies) as referred to under point 3.1 must...
4.3. The manufacturer(s) and, if involved the adjudicating entity or its...
4.4. The notified body(ies) must periodically carry out audits to make...
4.5. Additionally the notified body(ies) may pay unscheduled visits to the...
5. The manufacturer(s) and, if involved the adjudicating entity must, for...
6.1. The adjudicating entity or its authorised representative established within the...
6.2. The application must enable the design, manufacture, installation and operation...
6.3. The notified body must examine the application concerning the design...
6.4. The notified body must, concerning the other stages of the...
6.5. The notified body responsible for the EC verification, if not...
6.6. Where the subsystem meets the requirements of the TSI, the...
6.7. The notified body shall be responsible for compiling the technical...
7. The complete records accompanying the certificate of EC verification must...
8. The adjudicating entity or its authorised representative within the Community...
ASPECTS NOT SPECIFIC TO HIGH SPEED AND FOR WHICH NOTIFICATION OF NATIONAL RULES IS REQUIRED
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