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  2. AS9100 - Wikipedia

    en.wikipedia.org/wiki/AS9100

    The new standardized document, called 9100, was still based on ISO 9001:1994(E), although it was published separately by each country's aerospace association or standards body (AS 9100 in the U.S). AS 9100 added 55 aerospace industry specific amplifications and requirements to ISO 9001:1994. [10]

  3. First article inspection - Wikipedia

    en.wikipedia.org/wiki/First_article_inspection

    First Article Inspection is part of AS9145, Requirements for Advanced Product Quality Planning and Production Part Approval Process (APQP/PPAP), Phase 4 and is a required document for APQP/PPAP approval. See Production Part Approval Process.

  4. Business continuity and disaster recovery auditing - Wikipedia

    en.wikipedia.org/wiki/Business_continuity_and...

    The auditor examines records, billings, and contracts to verify that records are being kept. One such record is a current list of the organization's hardware and software vendors . Such list is made and periodically updated to reflect changing business practices and as part of an IT asset management system.

  5. Retention period - Wikipedia

    en.wikipedia.org/wiki/Retention_period

    A retention period (associated with a retention schedule or retention program) is an aspect of records and information management (RIM) and the records life cycle that identifies the duration of time for which the information should be maintained or "retained", irrespective of format (paper, electronic, or other). Retention periods vary with ...

  6. Inspection - Wikipedia

    en.wikipedia.org/wiki/Inspection

    In government and politics, an inspection is the act of a monitoring authority administering an official review of various criteria (such as documents, facilities, records, and any other assets) that are deemed by the authority to be related to the inspection. Inspections are used for the purpose of determining if a body is complying with ...

  7. Quality management - Wikipedia

    en.wikipedia.org/wiki/Quality_management

    ISO 13485 specifies Quality Management System requirements for organizations involved in the design and manufacture of medical devices to demonstrate the ability to meet relevant regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and ...

  8. Records management - Wikipedia

    en.wikipedia.org/wiki/Records_management

    Not all documents are records. A record is a document consciously (consciously means that the creator intentionally keeps it) retained as evidence of an action. Records management systems generally distinguish between records and non-records (convenience copies, rough drafts, duplicates), which do not need formal management.

  9. Allied Quality Assurance Publications - Wikipedia

    en.wikipedia.org/wiki/Allied_Quality_Assurance...

    The aim of the AQAP agreement is to define standards for Quality Assurance of defence products. These standards are an integral part of contracts awarded in the military field involving NATO member countries. AQAP documents are therefore important to contractors and companies wanting to bid for such contracts.

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