ISO 17025 2005 Awareness and Auditor Training Presentation Kit

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ISO/IEC17025-2005
LABORATORY ACCREDITATION
AWARNESS and Auditor training presentation
Product Code C107
Price 270 USD
www.globalmanagergroup.com
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ISO17025 2005 - SCOPE

• The requirements are
• The competence to carry out tests and or
  calibration and sampling.
• Applicable to all organization performing tests
  and or calibrations.
• To develop management system for quality,
  administrative and technical operations
• Applicable to all organisations

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OBJECTIVES OF ISO17025-2005

• The principles of good laboratory practice
  should be applied to all type of test laboratory
  having private or in house and in any
  manufacturing unit for testing
• To establish quality in testing and reliability
• To prevent risk
• To detect deviations
• To correct errors
• To improve efficiency

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MESSAGE FROM ISO 17025-2005

• Message in 5 lines for laboratories
• Say what you do
• Do what you say
• Record what you do
• Check the difference
• Act on the difference

Message in 1 line Do right thing, first time,
every time to achieve consistent quality Message
in 1 line Continual improvement is the way of
life
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Technical requirements

• Following factors determine the correctness and
  reliability of tests and or calibrations
• Accommodation and environment conditions
• Test and calibration methods and method
  validation
• Equipment
• Measurement traceability
• Sampling
• The handling of test and calibration Items

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BENEFITS OF ISO17025

• Establish confidence of management and customers
  on your test results as well as test reports and
  increase customer trust as well as market share.
• It will give better image of company as a Quality
  producer in Global market.
• Provide hot tips on analysis of data as well as
  measure uncertainty and perfect record keeping.
• Provide guideline for doing testing and
  measurement in detail.
• Provide guidelines and better control for
  maintenance of instruments, environment control,
  preservation of test records etc.

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CONTROL OF NONCONFORMING TESTING AND OR
CALIBRATION WORK

• The laboratory shall procedure for control of
  nonconforming testing and or calibration work
  which ensures that
• The responsibilities and authorities for
  management of non conforming work
• Significant evaluation of non conforming work
• Customer is notified and work is recalled
• The responsibilities for authorizing the
  resumption of work
• The follow up of corrective action procedure if
  required

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Accommodation and environmental condition

• The above facilities should be facilitate
  correct performance of the test and or
  calibrations
• The technical requirement for accommodation and
  environmental condition shall be documented
• Environmental condition shall be monitored,
  controlled and recorded
• Following shall be considered
• Biological sterility, dust, electromagnetic
  disturbance, radiation, humidity, electrical
  supply, temperature and sound and vibration
  levels as appropriate

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Handling of test and calibration items

• The laboratory shall have the procedure for the
• Transportation,
• Receipt,
• Handling,
• Protection,
• Storage,
• Retention and or disposal of test and
  calibration items
• Protection of the test or calibration items

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Equipment

• Use appropriate equipment
• Authorised personnel operate
• Instructions available
• Unique identification, inventory
• Equipment calibration
• Applies to outside equipment

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CONNECTIVITY OF GOOD LABORATORY PRACTICES( GLP)
AND CONFIRMATIVE ASSESSMENT AS PER ISO17025

• System
• Process
• Facility
• Personnel
• confidance