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IAF MD 5:2023 Determination of Audit Time of Quality, Environmental, and Occupational Health & Safety Management Systems Mandatory Documents (MD Series) 14 Jun 2023
The IAF MLA is structured in five levels: Level 1 specifies mandatory criteria that apply to all ABs, ISO/IEC 17011.
DETERMINATION OF AUDIT TIME OF QUALITY, ENVIRONMENTAL, AND OCCUPATIONAL HEALTH & SAFETY MANAGEMENT SYSTEMS. This document is mandatory for the consistent application of the relevant clauses of ISO/IEC 17021-1 for audits of quality, environmental and occupational health and safety management systems.
28 Απρ 2020 · IAF has also extended the application dates for Mandatory documents currently being implemented, the answer to FAQ 24 states “Yes, transition periods of all IAF mandatory documents are extended for six months. therefore, revised application dates are as follows: –. for IAF MD 5: 2019 – 7 November 2020. for IAF MD 17: 2019 – 7 November 2020.
14 Ιουν 2019 · Technical Bulletin – Recent Updates to IAF MD 5. This Technical Bulletin is applicable to all accredited management systems Certification Bodies and is to provide an update regarding recent changes to IAF document MD 5.
3 Μαΐ 2022 · In February 2022, the IAF Medical Devices Working Group (WG) completed a four-year cycle of improving one of the most important documents that supports the medical device quality system ISO 13485.
1) Purpose. This statement outlines the Irish National Accreditation Board’s policy regarding mandatory and. guidance documents for accredited and applicant organisations. 2) Guidance Documents.