The documents listed below are must-haves according to ISO 17025:2017. He was also a Managing Director and Senior Semiconductor Analyst at Alex Brown & Sons. Prior to TPG, he was a Managing Director and Co-Head, Technology Investment Banking Group at Morgan Stanley.
In this article, you’ll find a snapshot of what documents you need to have to be compliant with the 2017 revision of ISO 17025.īefore joining Temasek, John was a Partner of TPG Capital (“TPG”), where he led the firm’s Technology Buyout Team for 17 years. Whenever changes are applied to standards, the first questions that come to mind are: “Which documents are required?” and “How many documents are required?” For currently accredited systems, your questions may be something like: “What changes are required to our current documents?” or “What new documents do we need to generate to ensure compliance?” The ISO 17025:2017 standard actually requires fewer documents than the 2005 revision. The latest iteration of ISO 17025:2017 was revised for harmonization with ISO 9001:2015.
International Laboratory Accreditation Cooperation (ILAC) Mutual Recognition Arrangement (MRA. A2LA is governed by a Board of Directors. ISO/IEC 17020 for Inspection Bodies ISO/IEC 17043 for Proficiency Testing Providers. ISO/IEC 17025 for Testing/Calibration Laboratories ISO 15189 and CLIA for Clinical Testing Laboratories. R304 – General Requirements: ISO 17034 Reference Material Producer Accreditation Program R307 - General Requirements - Accreditation of ISO-IEC 17065 Product Certification Bodies R311 - Specific Requirements - Federal Risk and Authorization Management Program.
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