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  • Implementing Continual Improvement in a 17025 Laboratory

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Thursday - Jul 11, 2013 10:00 AM
  • End Time:
  • Thursday - Jul 11, 2013 12:00 PM
  • Location:
  • Online
  • This lab compliance training will provide tips and tricks on how to identify the issues that prevent laboratories from consistently producing technically valid results and address them in a way the prevents them from recurring.

    Why Should You Attend:

    ISO 17025 is used by laboratories as a standard to develop and establish a Quality System and for the assessment by their clients or by third parties. The standard is also being used as a criterion for laboratory accreditation.

    This 2-hr session will provide tips and tricks on how to identify the issues that prevent laboratories from consistently producing technically valid results and address them in a way the prevents them from recurring.

    Learning Objectives:

    - Upon completion of this course the attendee should:
    - Be familiar with the tools contained in 17025 to identify non-conformances, potential non-conformances and opportunities for improvement that are part of an accreditation body assessment.
    - Be familiar with the methods to address root causes with solutions that work for the laboratory.
    - Be familiar with the methods to follow up implementation of solutions for effectiveness in a manner that meets accreditation requirements.
    - Acquire simple forms to document (record) the steps from identification through root cause to implementation of solution and follow up that can impress any assessor.
    - Understand how to easily implement these approaches in a conformant laboratory quality system.
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