Paragraph 1
(1)
The manufacturer shall make an application in writing for evaluation of his quality system to a notified body.
(2)
The application shall be signed by or on behalf of the manufacturer and shall include—
(a)
the information and undertakings which are required by paragraph 2 of Schedule 5 to be included in an application under paragraph 1 of that Schedule, other than the information required by paragraph 2(1)(e) of that Schedule so far as it relates to research and development and design;
(b)
the technical documentation relating to the approved type and a copy of the EC type-examination certificate.