Understanding and Implementing ISO 17025
Instructor:
Dr. Ludwig Huber
Product ID: 700989
- Duration: 75 Min
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
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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