Test and Calibration Method Procedure (Clauses 7.2.1 & 7.2.2).Customer Service Procedure (Clauses 7.1.1 & 8.6).Equipment and Calibration Procedure (Clauses 6.4.3 & 6.5).Facilities and Environment Procedure (Clause 6.3).Externally Provided Products and Services Procedure (Clause 6.6.2).Competence, Training and Awareness Procedure (Clause 6.2.5).Document and Record Control Procedure (Clauses 8.2.1, 8.3 & 8.4).Nickelodeon Directors Lab Iso Download Windows 10 Keep in mind that if you exclude some of the clauses from the scope of your implementation, then documents for those clauses will not be required for your lab. 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.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. Archives
January 2023
Categories |