SN EN 62326-1 : 1997

1 Scope
2 Normative references
3 General
    3.1 General considerations
    3.2 Structure of the specification series
4 Particular stipulations
    4.1 Primary stage of manufacture
    4.2 Structurally similar printed boards
    4.3 Certified Records (CR) of released lots
    4.4 Delayed delivery
    4.5 Release for delivery before the completion of
          all tests
    4.6 Resubmission of rejected lots
    4.7 Marking of printed board and package
    4.8 Ordering information
5 Capability approval and maintenance of capability
    approval
    5.1 General
    5.2 Capability approval requirements
    5.3 Description of capability
    5.4 Register of Firms, Products and Services
          Information (RFPS)
    5.5 Demonstration of capability
    5.6 Capability approval test report
    5.7 Range of capability approval
    5.8 Maintenance of capability approval
    5.9 Suspension and withdrawal of capability approval
    5.10 Capability approval testing
    5.11 Inspection of information in the Cap DS
6 Quality assessment
    6.1 Quality conformance inspection
    6.2 Grouping of tests
    6.3 Inspection information in the CDS
    6.4 In-process testing and control
    6.5 Indirect measuring methods/process parameter
          control
7 Rules for the preparation of detail specifications
    7.1 Capability Detail Specification (Cap DS)
    7.2 Customer Detail Specification (CDS)
Annex A (informative) Examples of a CDS check list
Annex B (informative) Future Structure of the specification
        series
Annex C (informative) Structure of the capability
        qualifying component (CQC)
Annex D (informative) Abbreviations and acronyms related to
        IECQ and their explanations
Annex E (informative) Guide to the form and content of a
        capability manual
Annex F (informative) Example of process description
Annex G (informative) Example of limits of approval
Annex H (informative) Example of description of capability
Annex I (informative) Example of manufacturer-to-customer
        interface
Annex J (informative) Example of CQC detail specification
Annex K (informative) Example of test programme matrix
Annex L (informative) Example of test programme schedule
Annex M (normative) Requirements for capability approval
        test reports
Annex ZA (normative) Normative references to international
         publications with their corresponding European
         publications
Tables

Specifies capability approval (CA) procedures for printed boards, the information and requirements may also be used for second-party approvals or for self-declaration by a manufacturer of products.