Division 7.6 Where the conditions referred to in points (a) and (b) of point 7.4 are not met, a simplified review procedure shall apply. The manufacturer shall supply the approved body with the following:F1

1. (a)

   his name and address and data identifying the F2... type-examination certificate concerned;

2. (b)

   confirmation that there has been no modification to the approved type as referred to in point 7.2, including materials, sub-components or sub-assemblies, nor to the relevant F3designated standards or other technical specifications applied;

3. (c)

   confirmation that there has been no change in the state of the art as referred to in point 7.3;

4. (d)

   where not already supplied, copies of current product drawings and photographs, product marking and information supplied by the manufacturer; and

5. (e)

   for category III products, where not already available to the approved body, information on the results of the supervised product checks at random intervals carried out in accordance with Annex VII, or on the results of audits of his quality system carried out in accordance with Annex VIII.

Where the approved body has confirmed that no modification to the approved type referred to in point 7.2 and no change in the state of the art referred to in point 7.3 has occurred, the simplified review procedure shall be applied and the examinations and tests referred to in point 7.5 shall not be carried out. In such cases, the approved body shall renew the ... type-examination certificate.

The costs associated with that renewal shall be proportionate to the administrative burden of the simplified procedure.

If the approved body finds that a change in the state of the art referred to in point 7.3 has occurred, the procedure set out in point 7.5 shall apply.