Understanding and Implementing ISO 17025

Instructor: Dr. Ludwig Huber
Product ID: 700989
  • Duration: 75 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556


Read Frequently Asked Questions

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.

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 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 , 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:

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