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This is the original version as it was originally adopted in the EU.
This legislation may since have been updated - see the latest available (revised) version
The application must include:
name and address of the contracting entity or its authorised representative,
the technical documentation regarding the approved type, including the type examination certificate, as issued after completion of the procedure defined in module SB,
and, if not included in this documentation,
a general description of the subsystem, its overall design and structure,
the technical specifications, including European specifications, that have been applied,
any necessary supporting evidence for the use of the above specifications, in particular where these European specifications, and the relevant clauses have not been applied in full. This supporting evidence must include the results of tests carried out by the appropriate laboratory of the manufacturer or on his behalf,
the rolling stock register, including all information as specified in the TSI,
the technical documentation regarding the manufacture and the assembly of the subsystem,
evidence of conformity to other regulations deriving from the treaty (including certificates) for the production phase,
a list of the interoperability constituents to be incorporated into the subsys- tem,
copies of the EC declarations of conformity or suitability for use with which the constituents must be provided, and all the necessary elements defined in Annex VI to the Directives,
a list of manufacturers, involved in the subsystem's design, manufacturing, assembly and installation,
the demonstration, that all stages, as mentioned in point 5.2, are covered by quality management systems of the contracting entity, if involved, and/or of the main contractors, and the evidence of their effectiveness,
indication of the notified body, responsible for the approval and surveillance of these quality management systems.
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