| Axeon Corporation » Courses » ISO 17025

ISO 17025 Certified Lead and Internal Auditor Trainings

 laboratory-ISO-17025

What is ISO/IEC 17025:2005?

ISO/IEC 17025:2005 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods.

 

Who does ISO/IEC 17025:2005 apply to?

ISO/IEC 17025:2005 is applicable to all laboratories regardless of the number of personnel or the extent of the scope of testing and/or calibration activities. When a laboratory does not undertake one or more of the activities covered by ISO/IEC 17025:2005, such as sampling and the design/development of new methods, the requirements of those clauses do not apply.

 

Why is ISO/IEC 17025:2005 useful?

ISO/IEC 17025:2005 is for use by laboratories in developing their management system for quality, administrative and technical operations. Laboratory customers, regulatory authorities and accreditation bodies may also use it in confirming or recognizing the competence of laboratories. ISO/IEC 17025:2005 is not intended to be used as the basis for certification of laboratories.

 

Early Bird Pricing

 

• $200 off- 60 Days in Advance

 

• $100 off- 30 Days in Advance

 

5-Day ISO 17025 Lead Auditor with Testing and Calibration Focus: $1695

ISO 17025 36 (hr) Lead Auditor

 

Days: 5  • Price: $1795

 

Detailed Course Description

Develop your expertise and value as an ISO 17025 specialist. Review, write, and understand ISO 17025 nonconformances. Hone your skills; understand the rigors of the ISO/IEC 17025:2005 standard. Consultants will benefit from this course to help transition clients from other ISO standards to the requirements of ISO/IEC 17025.This course can also be invaluable as a refresher for long-time assessors of the ISO/IEC 17025 standard.

Learning Objectives

 

  • Understand all of the ISO/IEC 17025:2005 elements.
  • Cover the full range of assessment techniques and good practices.
  • Benefit from practical assessment exercises.
  • Gain an understanding and assessing uncertainty, traceability, and PT/ILC.
  • Get practical experience of planning, running, and reporting on assessments.

 

Who Should Attend

 

This course is for laboratory managers, laboratory technicians and laboratory technical staff, prospective assessors and consultants, and auditors of all types who want or need to learn better audit practices and want an appreciation for the technical demands of ISO/IEC 17025.

 

This course will help you:

 

  • Understand all of the ISO/IEC 17025:2005 elements.
  • Cover the full range of assessment techniques and good practices.
  • Benefit from practical assessment exercises.
  • Gain an understanding and assessing uncertainty, traceability, and PT/ILC.
  • Get practical experience of planning, running, and reporting on assessments.

 

Prerequisites

All attendees are required to bring their own copy of the ISO/IEC 17025:2005 standard to this course. These will not be provided for you. You can purchase a copy of this standard from ASQ (Item #T804).

Agenda

 

  1. Background of ISO 17025:2005
  2. Definitions, Terminology: ISO 9000, VIM etc.
  3. Assessment and Auditing Requirements: ISO 17011:2004, ISO 19011:2002, ISO 10012
  4. Logo and Symbol Use/Opening and Closing Meetings
  5. ILAC, IAAC, APLAC Recognition and Oversight
  6. ISO 17025 Requirements/Accreditation Requirements
    1. Clause 4 Review
      1. Case Studies on Clauses 4
      2. Review Clause 4 Case Studies
      3. Evening Assignments – Clause 4
  7. Accreditation Stages
  8. Document Review Exercise – Clause 5
  9. Auditing Guidelines – ISO 19011
  10. ISO 17025 Requirements
    1. Clause 5 Review
    2. Uncertainty (NIST 1297)- includes budgets and examples
  11. Traceability and PT/ILC
  12. ISO 17025 Scope of Accreditation
  13. Opening Meeting Activities
  14. Assessing ISO 17025 Using a Checklist
    1. Includes method witnessing /role playing
  15. Uncertainty Budget Software and example
  16. Case Studies: Uncertainty/PT/ILC/Traceability/Calibration Certificates
  17. Review of Assessment Case Studies and Certificate Shortcomings
  18. Assessment report Preparation
  19. Closing Meeting Participation Exercises
  20. Review of Standards and Assessment Requirements
  21. ACLASS-specific training, report types, assessor duties and resources available
  22. Practice Exam and Review
  23. Exam
  24. Audit Checklists and Audit reports
  25. Review of Standards and Internal Auditing issues
  26. Exam

 

As a member of your ISO 17025 project team, you gain critical knowledge to move your company ahead in today’s competitive marketplace. ISO Management Representatives will gain the credibility and prestige to effectively interact with certification bodies, customers, and suppliers. 

________________________________________________________________

This class is being taught and certified by ACLASS

3 Day Internal Auditor- $1395

3 Day Internal Auditor

by Exemplar Global (RABQSA) Auditors-Trainers

 

Days: 3 • CEU Hrs: 1.9

Day 1: 7:30 a.m.- 5:30 p.m.

Day 2: 7:30 a.m.- 4:00 p.m.

Day 3: 7:30 a.m.- 4:00 p.m.

Audience: Beginner to Advanced

 

Overview

This course prepares you to perform internal QMS audits using industry-proven techniques and to apply proper interpretation of the ISO standard to real life audit situations. You’ll follow the full audit process including: audit tools and preparation, opening meetings, audit interviews, closing meetings, and reporting.  This is a very practical class that is not “bogged-down” with academic discussions of quality topics that have limited utility for class attendees.

This class teaches Internal Auditing for ISO 9001, 13485, AS9100, TS 16949, and ISO 14001 Quality Management Systems.

This Internal Audit class makes extensive use of activities and case studies to help you fully understand the requirements of quality system auditing to the ISO 9001:2008 standard. Since people “lock” new understanding into long-term memory much better when they apply it, lecture time is held to a minimum providing you time to grasp and then practice your newly acquired skills in simulated real-life audit situations. 

Who Should Attend

Individuals who will perform audits to ISO 9001, 13485, AS9100, TS1649 and/or 14001 Standards or Quality Management Systems, individuals assisting their organizations toward ISO 9000 registration, or individuals who are frequently audited should attend this training. Quality directors, managers, engineers, auditors, ISO coordinators, laboratory quality professionals, and anyone engaged in quality audits will benefit from this training.

Prerequisites

There are no required prerequisites.  This course is routinely taught to quality novices and life-time professionals. All attendees are required to bring their own copy of the ISO 9001, 13485, AS9100, TS16949, and/or 14001 Quality Management Standard Requirements to this training course. These will not be provided for you. We strongly advise you bring a “paper” copy.

Course Objectives

  • Prepared to conduct a solo internal audit at successful course completion
  • Fully understand and interpret the ISO 9001:2015 requirements.
  • Apply the proper interpretation of the standard in actual audit situations.
  • Understand process auditing tools leading to substantive quality system improvements
  • Tailor an audit interview based on the requirements of the standard and obtain audit evidence from this interview.
  • Follow-up and resolve “audit trails that present themselves during the audit interviews
  • Conduct audits that result in real improvements to the quality system
  • Plan and execute the entire audit process including: audit preparation, opening meetings, auditing, closing meetings, and reporting.

 

Agenda

 

 Part 1: Introductions and Self-Assessment

  • Course requirements
  • How to get the most from this experience
  • Networking with class mates (industry professionals)
  • Self-assessment of audit skills and internal audit programs Exercise #1

 

Part 2: Quality Terminology and Definitions

  • Quality industry vernacular from ISO 9000, ISO 19011
  • Differentiating between Verification and Validation
  • Understanding Corrective and Preventive Actions
  • How to converse with external auditors
  • Terminology Exercise #2

 

Part 3: Requirements of ISO 9001:2015

  • Demystifying the ISO 9001 standard
  • Interpreting and cross-referencing the quality standard
  • Analyzing audit findings
  • Audit exercises for application of ISO 13485 to quality events
  • Exercise #3-#7: Short case studies in quality events

 

Part 4: The Audit Process: Roles and Duties

  • Roles of Auditors, Auditees, and Management during Internal Audits (IAs)
  • Qualifying Auditors
  • Duties of the IA staff
  • Exercise #8: Preparing to be audited

 

Part 5: The Audit Process: Performing the Audit Process

  • Audit Tools – checklists, process maps, findings, reports
  • Conducting Audit Interviews Exercise #9
  • Exercise #10 Quality event case studies

 

Part 6: The Audit Process: Audit Skills and Techniques

  • Audit Interviewing techniques
  • Continual improvement techniques
  • Process Auditing methods
  • Developing a “continual improvement” attitude in the organization
  • Exercise #11 Writing Audit Findings
  • Exercise #12 Evaluating the effectiveness of Audits
  • Exercise #13 Application of Process Auditing techniques

 

Part 7: The Audit Process: Finalizing the Audit

  • Writing the audit report
  • Opening and Closing Meetings
  • Exercise #14 Writing and audit report
  • Exercise #15 Writing Non-Conforming Reports
  • Exercise #16 Conducting a Closing Meeting

 

Review and Examination for Certificate