Understanding and Implementing ISO 17025

Instructor: Dr. Ludwig Huber
Product ID: 700989
  • Duration: 75 Min
This webinar will provide a detailed information on the critical requirements of ISO 17025 and recommendations for cost effective implementation. You will learn steps towards laboratory accreditation and how to prepare for an ISO 17025 audit.

recorded version

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Last Recorded Date: Aug-2012

Training CD / USB Drive

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Course "Understanding and Implementing ISO 17025" has been pre-approved by RAPS as eligible for up to 1 RAC credits towards a participant's RAC recertification upon full completion.

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. ISO 17025 is applicable to all organizations performing tests and/or calibrations, regardless of the number of personnel or the extent of the scope of testing and/or calibration.

This webinar gives a detailed information on the critical requirements of ISO 17025 and recommendations for cost effective implementation.


For easy implementation, attendees will receive

  • Laboratory Quality Manual: Template and examples
  • ISO17025: Step-by-step implementation

Note: These complimentary hand-outs will be sent to customers on request. Please email customercare@complianceonline.com for these documents, stating your order number, and they will be emailed to you within 4 working days.

Areas Covered in the Seminar:

  • Benefits of ISO 17025.
  • Management requirements.
  • Technical requirements.
  • Documentation requirements.
  • Steps towards ISO 17025 laboratory accreditation.
  • ISO 17025 and agencies, such as US FDA.
  • Impact on Analytical Laboratories.
  • Recommendations for implementation.
  • Dealing with multiple quality systems.
  • Preparation for an ISO 17025 Audit.
  • Local and global resources.

Who will Benefit:

The following personnel from food, environmental, clinical and chemical testing laboratories will benefit:

  • Food, environmental, chemical, clinical testing laboratories
  • QA managers and personnel
  • Analysts and lab managers
  • Training departments
  • Documentation department
  • Consultants

Instructor Profile:

Dr. Ludwig Huber , Ph.D., is Director of Labcompliance and Chief Advisor for global FDA compliance at Agilent Technologies. He is the editor of www.labcompliance.com , the global on-line resource for validation and compliance issues for laboratories. He is the author of the books “Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems", Informa Healthcare. For more information, visit Dr. Huber's website: www.ludwig-huber.com

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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