Understanding and Implementing ISO 17025

Speaker

Instructor: Dr. Ludwig Huber
Product ID: 700989

Location
  • 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 TRAINING
Last Recorded Date: Aug-2012

 

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Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
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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.

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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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. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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