CATEGORY TYPE: Quality & Auditing

COURSE NAME:ISO 17025-2005 for Laboratory Quality System


UPCOMING EVENTS


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This course can be scheduled at your convenience, to request this course please click here
INTRODUCTION:
  • This course is a comprehensive look at ISO 17025 and its documentation and internal auditing requirements. Previously taught in three separate one-day courses, the merged subject matter enables the instructor to present an understandable explanation of the standard and how it should be applied. In this course, you will gain critical insight on the interpretation of the requirements of this new laboratory standard and you will also receive a detailed review of the accreditation process.
OBJECTIVES:
  • You will learn how to design and develop laboratory documents and quality manuals. The quality manual will be examined as to its impact on laboratory operations and what purpose it serves. You will learn what information it should contain, what writing style is most effective and how to keep your documents and quality manual up to date.
    • This course also gives attendees the knowledge needed to establish an internal quality audit program as required by ISO 17025, and to initiate the sequence of activities involved in scheduling, planning, conducting, reporting on and closing out internal quality audits. Participants will be able to employ effective techniques of auditing and the ability to develop the auditing procedures, scheduling and recording systems needed to sustain the program.
    • Attendees will receive practical instructions on the development, implementation and long-term maintenance of an effective laboratory quality system.
OUTLINE:

 

Day One:

ISO/IEC 17025:2005 What the Standard Requires

  • Background of standard
  • Objectives of ISO 17025
  • Application of ISO 17025
  • Management requirements
  • Technical requirements
  • Assurance of test results
  • Proficiency
  • Inter lab compression
  • Measurement uncertainty
  • Documentation requirements of ISO 17025
  • How to prepare quality manual
  • How to determine scope of accreditation

 

Day Two:

ISO/IEC 17025:2005 What the Standard Requires

  • Quality system
  • Subcontractor quality
  • Equipment control
  • Maintenance
  • Training
  • Calibration
  • Traceability
  • Test procedures
  • Sample preparation
  • Nonstandard samples
  • Environmental conditions
  • Reports
  • Document control, maintenance, storage and disposal
  • The auditing and accrediting process

 

Day Three:

Preparation of Documentation:

  • Documentation Requirements
  • How to design a quality manual
  • Effective documentation control
  • Auditing a sample quality manual

 

Day Four:

Internal audits of the lab:

  • What is an internal audit; why it's important
  • What should it accomplish
  • How should the program be organized; steps

 

Day Five:

  • How should effort be coordinated
  • Establishing/managing audit program
  • Planning/conducting the audit
  • Effective questioning techniques
WHO SHOULD ATTEND:
  • Quality Managers, Lab Managers, Lab Assistants and Staff.
DURATION:
    • 5 Day(s)
  •  


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    Sabic

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    Sabic

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    Sabic

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    Sabic

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    Mobily

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    General Authority of Civil Aviation (GACA)

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    Sabic

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    Sabic

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    Al-Suwadi Services

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    Coldstorec Group Of Saudi Arabia

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    Saudi Aramco

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    Al-Suwadi Services

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    Al Khodari Company

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    Al Khodari Company

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    Al Khodari Company

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    Al Khodari Company