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Documents
  • Approval of manufacturing process
    • (A) The manufacturer wishing to obtain the approval of manufacturing process is to submit a copy of the application of approval for manufacturing process of the Society together with three copies of the required data for the approval and two copies of the required data for reference to the Society.
    • (B) Data to be submitted
      • a) Data for approval
        • Test plan for the approval of manufacturing process and applicable standard, codes or rules (Where test methods and procedure are specified into this Guidance, IMO Res., KS standard, etc., the data to indicate the related standard instead of this required data may be submitted except detail drawings of test specimens.)
      • b) Data for reference
        • (A) Details of products information
          • (a) Type of products, grade of steel, thickness and specification of products
        • (B) Outline of workshops
          • (a) Name and address of the manufacturer, history, layout and dimension of works
        • (C) Organization and quality
          • (a) Organizational chart and staff employed
          • (b) Staff employed and organization of the quality control department
          • (c) Qualification of the personnel involved in activities related to the quality of the products
          • (d) Certification of compliance of the quality system with IS0 9001, if any.
          • (e) Approval certificates already granted by other Classification Societies, if any.
        • (D) Manufacturing facilities
          • (a) Flow chart of the manufacturing process
          • (b) Origin and storage of raw materials
          • (c) Storage of finished products
          • (d) Equipment for systematic control during fabrication
        • (E) Details of inspections and quality control facilities
          • (a) Details of system used for identification of materials at the different stages of manufacturing
          • (b) Equipment for mechanical tests, chemical analyses and metallography, non destructive examinations and relevant calibration procedures
          • (c) List and documents for inspection and testing
        • (F) Service records
          - Estimated total annual production of finished products for shipbuilding and for other applications
        • (G) Other data deemed necessary by the Society
    • C) Notwithstanding the requirements, where the applicant is already approved by the Society and then attachments are entirely equal in content to the documents previously submitted to the Society, the documents may be partly or entirely exempted from submission except for approval test program for approval of the manufacturing process.
  • Type Approval
    • A) The manufacturer wishing to obtain a type approval is to submit a copy of the application of type approval of the Society, together with three copies of the required data for approval and two copies of the required data for reference, to the Society. However, the required data previously submitted to the Society, according to the Technical Rules, may be exempted from submission.
    • B) Data to be submitted
      • a) Data for approval
        • Type test program and applicable standards, codes or rules (when the test methods, procedures, etc. in the Guidance, IMO Resolution, Korean Industrial Standards, etc. apply, their number and subject stipulation instead of submission may be accepted except details of test specimens.)
      • b) Relevant drawings (sectional assembly, drawings for main component parts) and documents
      • c) Data for reference
        • (A) Particulars and specifications of products
        • (B) Data on history, outline and layout of manufacturing plants
        • (C) When examination of works is required, the following reference data may be submitted.
          • (a) Data on major manufacturing facilities
          • (b) Data on manufacturing process
          • (c) Data of in-house standards or codes
          • (d) Data of quality control system
          • (e) Data on major inspection and testing facilities
          • (f) Service records
          • (g) List of subcontractors and their products
          • (h) For a newly developed product, documents related to tests and their results for its development
    • C) Notwithstanding the requirements, where the applicant is already approved by the Society and the attachments are entirely equal in content to the documents previously submitted the submission of documents may be partly or wholly exempted except for the approval test program.
  • Design Approval
    • A) The manufacturers wishing to obtain design approval are to submit a copy of the application of design approval and for approval, three copies and for reference, two copies of the drawings and documents of machinery and equipment according to applicable Rules.
    • B) Drawings and data to be submitted
      • a) Name of products
      • b) Type and model number
      • c) Specification of products (for reference)
      • d) List of drawings and documents submitted
      • e) Operating manual (for reference)
    • C) When the alteration of the specification, construction, etc. is to be made on the machinery and equipment which have been granted the design approval, the manufacturer is to submit the application of alteration to the Society together with the detailed drawings and documents of the alteration.
  • Approval of Quality Assurance System
    • A) The manufacturers wishing to the approval of quality assurance system are to submit a copy of the application of approval of quality assurance system together with following data to the Society.
    • B) Data to be submitted
      • (a) Quality Manual : 3 copies
      • (b) A list of internal quality system procedures : 1 copy
      • (c) Outline of the products to which the quality assurance system is applied (product name, range of application for approval, etc.) : 1 copy
      • (d) Applicable codes, inspection & testing plan : 1 copy
      • (e) Personal records of education and experience in charge of manufacturing survey : 1 copy
      • (f) Other data deemed necessary by the Society for the approval of quality assurance system
  • Manufacturer Approval
    • A) The manufacturers wishing to obtain the Manufacturer Approval are to submit a copy of the application of the Manufacturer Approval and two copies of data in Ch 3, 102. 3(2)to the Society.
    • B) The manufacturers of paints and fire protection materials, etc. wishing to the first time plant audit for the Manufacturer Approval are subjected to be together with typeapproval.
    • C) The manufacturers wishing to the Periodical Audit and Renewal Audit of manufacturerapproval are to submit a copy of the application of the Manufacturer Approval togetherwith following data to the Society.
      • Reviewed manufacturing process during previous plant audit, the specification and list of the alteration to the manufacturing facilities(where practicable, to be mentionedwith a comparison table form between new and old)
      • (b) List of Type Approved Equipment issued by the Society
      • (c) The copies for test records and the date list of accuracy and calibration of inspectionand testing facilities
      • (d) Service records to the Society
      • (e) For the manufacturer of equipments components, documents specified the relationshipwith manufacturers of final assembly
    • D) However, the required data previously submitted to the Society, according to theTechnical Rules, may be exempted from submission.