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  2. File:Mainstreaming internal quality assurance with management.pdf

    en.wikipedia.org/wiki/File:Mainstreaming...

    If the file has been modified from its original state, some details may not fully reflect the modified file. Short title Mainstreaming internal quality assurance with management: University of Talca, Chile; New trends in higher education: case study; 2017

  3. File:Towards Quality Assurance.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Towards_Quality...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  4. File:From Externally to Internally Driven Quality Assurance.pdf

    en.wikipedia.org/wiki/File:From_Externally_to...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate

  5. QA/QC - Wikipedia

    en.wikipedia.org/wiki/QA/QC

    QA/QC is the combination of quality assurance, the process or set of processes used to measure and assure the quality of a product, and quality control, the process of ensuring products and services meet consumer expectations.

  6. Quality assurance - Wikipedia

    en.wikipedia.org/wiki/Quality_assurance

    The terms "quality assurance" and "quality control" are often used interchangeably to refer to ways of ensuring the quality of a service or product. [3] For instance, the term "assurance" is often used in a context such as: Implementation of inspection and structured testing as a measure of quality assurance in a television set software project ...

  7. Quick access recorder - Wikipedia

    en.wikipedia.org/wiki/Quick_access_recorder

    QARs are typically used by airlines to improve flight safety and operational efficiency, usually in the scope of their flight operational quality assurance plans. [4] Like the aircraft's flight data recorder (FDR), a QAR receives its inputs from the Flight Data Acquisition Unit (FDAU), recording over 2000 flight parameters. [1]

  8. Device Master Record - Wikipedia

    en.wikipedia.org/wiki/Device_Master_Record

    Design History File (DHF) The sub-clause 4.2.3 of ISO 13485 :2016 requires a manufacturer of medical device to establish a Technical file , similar to a device master record. The EU medical device regulation requires a manufacturer of a medical device to maintain a Technical documentation .

  9. Quality control - Wikipedia

    en.wikipedia.org/wiki/Quality_control

    Quality inspector in a Volkseigener Betrieb sewing machine parts factory in Dresden, East Germany, 1977. Quality control (QC) is a process by which entities review the quality of all factors involved in production. ISO 9000 defines quality control as "a part of quality management focused on fulfilling quality requirements". [1]