The Merchant Shipping (Marine Equipment) Regulations 2025
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Change 1
10 United Kingdom conformity approval: obligations of an approved body
(1) An approved body must— (a) decide whether to grant or refuse United Kingdom conformity approval in accordance with the provisions of Schedule 2; and (b) where an application is made under Part 1 (module B) of Schedule 2, produce an evaluation report recording the activities undertaken in accordance with paragraph 5 of that Schedule and their outcomes. (2) Where an approved body grants United Kingdom conformity approval, it must— (a) for the conformity approval of equipment under Part 1 (module B) of Schedule 2, issue a certificate containing the information specified in paragraph 6 of Schedule 2; (b) for approval of a quality system under Part 2 (module D) or Part 3 (module E) of Schedule 2, notify the manufacturer of its decision in writing, including the conclusions of the audit of the quality system and the reasons for its decision; or (c) where verifying a product under Part 4 (module F) or Part 5 (module G) of Schedule 2, issue a certificate of conformity pursuant to Part 4 or Part 5 for that product. (3) Where an approved body refuses United Kingdom conformity approval, it must notify the manufacturer in writing, giving detailed reasons for its decision. (4) An approved body must— (a) periodically audit a quality system that it has approved; and (b) provide the manufacturer with a report containing the results of the audit. (5) Following the grant of United Kingdom conformity approval, an approved body must comply with the provision of information requirements in Schedule 2 and must inform the Secretary of State about any refusal, restriction, suspension or withdrawal of a conformity certificate and, on request, information about the conformity assessment activities performed within the scope of that approved body's designation, and any other activity performed.
10 United Kingdom conformity approval: obligations of an approved body
(1) An approved body must— (a) decide whether to grant or refuse United Kingdom conformity approval in accordance with the provisions of Schedule 2; and (b) where an application is made under Part 1 (module B) of Schedule 2, produce an evaluation report recording the activities undertaken in accordance with paragraph 5 of that Schedule and their outcomes. (2) Where an approved body grants United Kingdom conformity approval, it must— (a) for the conformity approval of equipment under Part 1 (module B) of Schedule 2, issue a certificate containing the information specified in paragraph 6 of Schedule 2; (b) for approval of a quality system under Part 2 (module D) or Part 3 (module E) of Schedule 2, notify the manufacturer of its decision in writing, including the conclusions of the audit of the quality system and the reasons for its decision; or (c) where verifying a product under Part 4 (module F) or Part 5 (module G) of Schedule 2, issue a certificate of conformity pursuant to Part 4 or Part 5 for that product. (3) Where an approved body refuses United Kingdom conformity approval, it must notify the manufacturer in writing, giving detailed reasons for its decision. (4) An approved body must— (a) periodically audit a quality system that it has approved; and (b) provide the manufacturer with a report containing the results of the audit. (5) Following the grant of United Kingdom conformity approval, an approved body must comply with the provision of information requirements in Schedule 2 and must inform the Secretary of State about any refusal, restriction, suspension or withdrawal of a conformity certificate and, on request, information about the conformity assessment activities performed within the scope of that approved body's designation, and any other activity performed.
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