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  2. IATF 16949 - Wikipedia

    en.wikipedia.org/wiki/IATF_16949

    A key requirement of IATF 16949:2016 is the fulfillment of customer-specific requirements, set up by the automotive manufacturer in addition to the quality management system of their suppliers. This may have decisively contributed to the worldwide recognition of the IATF standard by many manufacturers.

  3. Advanced product quality planning - Wikipedia

    en.wikipedia.org/wiki/Advanced_product_quality...

    Advanced product quality planning (APQP) is a framework of procedures and techniques used to develop products in industry, particularly in the automotive industry. It differs from Six Sigma in that the goal of Six Sigma is to reduce variation but has similarities to Design for Six Sigma (DFSS).

  4. International Automotive Task Force - Wikipedia

    en.wikipedia.org/wiki/International_Automotive...

    Its aim is to "provide improved quality products to automotive customers worldwide". [1] According to the IATF, the specific purposes for which the IATF were established are: Develop a consensus regarding international fundamental quality system requirements for production materials, products and services (e.g., heat treating, painting and ...

  5. QS9000 - Wikipedia

    en.wikipedia.org/wiki/QS9000

    On December 14, 2006, all QS9000 certifications were terminated. With QS9000, the middle certification between ISO 9001 and ISO/TS 16949, no longer valid, businesses had a choice between either ISO9001 or TS16949. QS9000 is considered superseded by ISO/TS 16949, now a standard published by IATF, thus renamed IATF 16949:2016 (current version).

  6. Quality management system - Wikipedia

    en.wikipedia.org/wiki/Quality_management_system

    Quality management software centralizes the storage of these documents. Regulatory compliance: To decrease compliance risks, quality management software is used within companies to make sure they comply with ISO, OSHA, FDA, and other industry norms and requirements. The software makes closed-loop corrective and preventive action procedures ...

  7. DEPARTMENT OF HEALTIl AND HUMAN SERVICES FOOD AND DRUG ...

    highline.huffingtonpost.com/miracleindustry/...

    • no Quality otl lea lOn was llnp emente regar mg t ere] ec IOn 0 contammated b. QA and Compliance Department overall responsibilities per the firm's deficient as follows: It does not maintain adequate laboratory facilities or e stmg an approval (or rejection) of components and drug products; it neglects review and approval ofvalidation