Αποτελέσματα Αναζήτησης
This webinar gave a brief overview of IAF informative and mandatory documents. It was presented by James Stapleton, Assessment Manager with INAB.
12 Ιαν 2024 · As of January 7, 2024, the International Accreditation Forum's Mandatory Document, "IAF MD 25: Criteria for the Evaluation of Conformity Assessment Schemes,"...
The scope of the IAF MLA is detailed in the IAF MLA Status document. The IAF MLA is structured in five levels: Level 1 specifies mandatory criteria that apply to all ABs, ISO/IEC 17011.
This course is suitable for certification bodies and covers the mandatory requirements and guidance for the determination of audit time for audits of QMS, EMS, and OH&SMS. The purpose of this course is to increase overall understanding of, and ability to implement the requirements of IAF MD 5.
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 · How Does This Help the Medical Device Industry? Some regulators are now demanding that the ‘legal manufacturers’ pay much closer attention to ‘critical suppliers’. IAF MD 9:2022 improves audits of ‘critical suppliers’ by using audit teams that carry technical expertise related to medical devices.
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.
