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UK approved recommendation UK25/G001 on the early application of available testing standards before their inclusion into MSN 1874. Adopted EU recommendation GEN-059.
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UK approved recommendation UK23/G002 on the use of Authorised Representatives, and what evidence needs to be supplied to Approved Bodies.
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UK approved recommendation UK23/G001 on issuing ‘own brand’ certificates – i.e., those bought from the original manufacturer and then sold on by a second manufacturer under the second manufacturer’s own branding.
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Adopted EU recommendation GEN-001. UK approved recommendation on the format of Module B certificates.
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Adopted EU recommendation GEN-002. UK approved recommendation on the assessment of Modules D, E, F and G.
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Adopted EU recommendation GEN-005. UK approved recommendation on the issuing of Module G certificates.
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Adopted EU recommendation GEN-003. UK approved recommendation on how to obtain product surveillance certification by several UK Approved Bodies.
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Adopted EU recommendation GEN-006. UK approved recommendation on period of validity of a UK certificate of conformity.
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Adopted EU recommendation GEN-007. UK approved recommendation UK21/G007 on the issuing of certificates to multiple applicants for the same product.
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Adopted EU recommendation GEN-010. UK approved recommendation on testing standards and the responsibilities of UK Approved Bodies.
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Adopted EU recommendation GEN-013. UK approved recommendation on the issuing of one conformity assessment certificate to cover multiple modules.
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Adopted EU recommendation GEN-019. UK approved recommendation on the application a standardised template for conformity assessment reports and certificates.
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Adopted EU recommendation GEN-020. UK approved recommendation UK21/G011 on tests conducted by Recognised Organisations.
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Adopted EU recommendation GEN-037. UK approved recommendation on the testing of an item of marine equipment that functions as a component part of a system.
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Adopted EU recommendation GEN-040. UK approved recommendation on the process to be followed when a new product is added to module D or E.
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Adopted EU recommendation GEN-041.UK approved recommendation on the actions to take should a product failure be detected during periodical surveillance or an unannounced visit.
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Adopted EU recommendation GEN-042. UK approved recommendation on the new requirements for manufacturers and UK Approved Bodies following amendments to testing standards.
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Adopted EU recommendation GEN-046. UK approved recommendation on the role of the Approved Body in risk assessment.
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Adopted EU recommendation GEN-048. UK approved recommendation on how to display the date when affixing the UK conformity mark to a piece of equipment.
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Adopted EU recommendation GEN-049. UK approved recommendation on the correct application of the UK conformity mark (the “Red Ensign”).
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Adopted EU recommendation GEN-034. UK approved recommendation on the certification of products with more than one marketing name.
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Adopted EU recommendation GEN-029. UK approved recommendation on the capturing of performance criteria identified during type examination.
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Adopted EU recommendation GEN-027. UK approved recommendation on the steps to be undertaken for the issuance and maintenance of Module F.
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Adopted EU recommendation GEN-025. UK approved recommendation on systems with functions other than those required.
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Adopted EU recommendation GEN-021. UK approved recommendation on the responsibility of UK Approved Bodies for testing conducted by independent laboratories.
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Adopted EU recommendation GEN-047. UK approved recommendation on the correct methods of type approval.
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Adopted EU recommendation GEN-050. UK approved recommendation on the issuance of safety information by manufacturers.
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Adopted EU recommendation GEN-036. UK approved recommendation on the use of product design licences.