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  2. Continual improvement process - Wikipedia

    en.wikipedia.org/wiki/Continual_improvement_process

    The term "continual improvement", not "continuous improvement", is used in ISO 14000, and is understood to refer to an ongoing series of small or large-scale improvements which are each done discretely, i.e. in a step-wise fashion. Several differences exist between the CIP concept as it is applied in quality management and environmental management.

  3. ISO 14000 family - Wikipedia

    en.wikipedia.org/wiki/ISO_14000_family

    The ISO 14000 family is a set of international standards for environment management systems. ... These recommendations are incorporated through continual improvement ...

  4. Quality management system - Wikipedia

    en.wikipedia.org/wiki/Quality_management_system

    Organizations can participate in a continuing certification process to ISO 9001:2015 to demonstrate their compliance with the standard, which includes a requirement for continual (i.e. planned) improvement of the QMS, as well as more foundational QMS components such as failure mode and effects analysis . [6]

  5. Quality management - Wikipedia

    en.wikipedia.org/wiki/Quality_management

    Improvement must allow pauses between implementing new changes so that the change is stabilized and assessed as a real improvement before the next improvement is made (hence continual improvement, not continuous improvement). Improvements that change the culture take longer as they have to overcome greater resistance to change.

  6. Total quality management - Wikipedia

    en.wikipedia.org/wiki/Total_quality_management

    "Top management has direct responsibility for quality improvement." "Increased quality comes from systematic analysis and improvement of work processes." "Quality improvement is a continuous effort and conducted throughout the organization." The Navy used the following tools and techniques: The PDCA cycle to drive issues to resolution

  7. ISO 9000 family - Wikipedia

    en.wikipedia.org/wiki/ISO_9000_family

    ISO 13485:2016 is a stand-alone standard. Because ISO 13485 is relevant to medical device manufacturers (unlike ISO 9001, which is applicable to any industry), and because of the differences between the two standards relating to continual improvement, compliance with ISO 13485 does not necessarily mean compliance with ISO 9001 (and vice versa).

  8. Environmental management system - Wikipedia

    en.wikipedia.org/wiki/Environmental_management...

    The diagram shows the process of first developing an environmental policy, planning the EMS, and then implementing it. The process also includes checking the system and acting on it. The model is continuous because an EMS is a process of continual improvement in which an organization is constantly reviewing and revising the system. [8]

  9. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    While it remains a stand-alone document, ISO 13485 is generally harmonized with ISO 9001.A principal difference, however, is that ISO 9001 requires the organization to demonstrate continual improvement, whereas ISO 13485 requires only that the certified organization demonstrate the quality system is effectively implemented and maintained.

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