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ISO 15189. ISO 15189 Medical laboratories — Requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organisation for Standardization 's Technical Committee 212 (ISO/TC 212).
Website. www.iso.org. The International Organization for Standardization (ISO / ˈaɪsoʊ / [3]) is an independent, non-governmental, international standard development organization composed of representatives from the national standards organizations of member countries. [4] Membership requirements are given in Article 3 of the ISO Statutes.
ISO 1 – ISO 1999. ISO 2000 – ISO 2999. ISO 3000 – ISO 4999. ISO 5000 – ISO 7999. ISO 8000 – ISO 9999. ISO 10000 – ISO 11999. ISO 12000 – ISO 13999. ISO 14000 – ISO 15999. ISO 16000 – ISO 17999.
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PDF/UA (PDF/Universal Accessibility), [1] formally ISO 14289, is an International Organization for Standardization (ISO) standard for accessible PDF technology. A technical specification intended for developers implementing PDF writing and processing software, PDF/UA provides definitive terms and requirements for accessibility in PDF documents and applications. [2]
The ISO 14000 family of standards by the International Organization for Standardization (ISO) relate to environmental management that exists to help organizations (a) minimize how their operations (processes, etc.) negatively affect the environment (i.e. cause adverse changes to air, water, or land); (b) comply with applicable laws, regulations, and other environmentally oriented requirements ...
ISO 14155:2011 Clinical investigation of medical devices for human subjects – Good clinical practice. ISO 14163:1998 Acoustics – Guidelines for noise control by silencers. ISO 14164:1999 Stationary source emissions – Determination of the volume flowrate of gas streams in ducts – Automated method.
In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. In many cases, suppliers and regulatory authorities will not accept test or calibration results from a lab that is not accredited. Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by ...