![]() Understand the new concepts of impartiality, risk management and risk evaluation techniques, decision rule, and process approach.Get ready-to-use internal audit checklists with clause-wise questions to perform an effective audit. ![]() Gain knowledge of internal auditing and use of audit checklists.Understand the required documentation, list of procedures and records required and how to audit them.Understand general and structural requirements of the ISO/IEC 17025:2017 standard.Get an overview of ISO/IEC 17025:2017 laboratory management system (LMS) and the benefits to implement it.Become familiar with ISO 17025:2017 laboratory management system requirements clauses and sub clauses.Auditors (Internal, 3rd Party, and Supplier).ISO Managers/Management Representatives.Professionals working in or with a Laboratory.This course is intended particularly for laboratories or organizations that work closely with laboratories to develop effective management systems that conform to ISO/IEC 17025. Numerous hands-on audit activities, including developing and using checklists, are incorporated throughout the course to allow participants to begin to leverage their knowledge gained during the course. In this course participants will be introduced to the principles of auditing, will be provided with an approach for developing, implementing, and managing an audit program, will learn the audit process and several audit methods for collecting, verifying, and recording objective evidence, and will discuss audit risks. This ISO/IEC 17025 training course provides a detailed review of ISO/IEC 17025:2017 as well as a review of ISO 19011, Guidelines for Auditing Management Systems. An audit program is also essential and required to achieve and maintain accreditation. Technical Requirements includes factors that determine the correctness and reliability of the tests and calibrations performed by the laboratory.Īn integral part of a successful management system is an effective audit program. Management Requirements are primarily related to the operation and effectiveness of the laboratory’s quality management system. The two main sections are Management Requirements and Technical Requirements. ISO/IEC 17025:2017 consists of five elements: Scope, Normative References, Terms and Definitions, Management Requirements, and Technical Requirements. It covers testing and calibration quality systems using standard methods, non-standard methods, and laboratory-developed methods. ISO/IEC 17025 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. MA Workforce Training Fund Express Grant.MA Workforce Training Fund General Grant.Outsourced PPAP Review & Disposition (APQP Processes).Auditing Core Tools & Customer-Specific Requirements.Quality / Regulatory Management Systems.EU’s In Vitro Diagnostic Medical Devices Regulation (IVDR).Cybersecurity Maturity Model Certification (CMMC).Process Improvement Tools / Technical Skills.Quality Management & Quality Control Support Services.National Aerospace and Defense Contractors Accreditation Program (NADCAP).Management System Standards – Implementation & Integration.
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