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The ISO 9000 family is a set of international standards for quality management systems.It was developed in March 1987 by International Organization for Standardization.The goal of these standards is to help organizations ensure that they meet customer and other stakeholder needs within the statutory and regulatory requirements related to a product or service.
The CAO supervises the management of public-sector companies and government departments, including about 130 central government departments and administrative units, 120 service agencies, 27 governorates, 50 economic authorities and more than 160 state-owned enterprises, political parties, trade unions, national and party news media, and all units subsidised by the State.
Facility management [1] or facilities management (FM) is a professional discipline focused on coordinating the use of space, infrastructure, people, and organization. Facilities management ensures that physical assets and environments are managed effectively to meet the needs of their users.
Australian Council on Healthcare Standards International (ACHSI) [7] Australian General Practice Accreditation Limited (AGPAL) [8] Australian Commission on Safety and Quality in Health Care (ACSQHC) [9] uses standards developed by the National Safety and Quality Health Service Standards (NSQHS Standards) [10]
ISO/TS 55010: Guidance on alignment of asset management, finance and accounting (published in September 2019, see below) ISO 55011: Guidance on the development of government asset management policy (targeted for 2021) ISO 55002:2018. In November 2018 a revised and expanded version ISO 55002:2018 was released. [7]
The ISO/IEC 27001 certification, like other ISO management system certifications, usually involves a three-stage external audit process defined by ISO/IEC 17021 [11] and ISO/IEC 27006 [12] standards: Stage 1 is a preliminary review of the ISMS. It includes checks for the existence and completeness of key documentation, such as the organization ...
In its Guidance for Industry "Data Integrity and Compliance With Drug CGMP" US-FDA states “it is the role of management with executive responsibility to create a quality culture where employees understand that data integrity is an organizational core value and employees are encouraged to identify and promptly report data integrity issues ...
product certifications (many nations) Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).