Laboratory Compliance 2012 - Understanding and Implementing ISO 17025
Date2012-06-20
Deadline2012-06-20
VenuePalo Alto, USA - United States
KeywordsISO 17025 compliance training; good laboratory practices compliance training; ISO training; quality system compliance; ISO laboratory standards
Topics/Call fo Papers
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.
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.
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.
Other CFPs
- Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus)
- Calibration and Qualification in Analytical Laboratories
- International Workshop on Infrastructure, Technologies and Applications for Distributed Data Collection, Processing and Dissemination
- The Third International Conference on Tourism and Hospitality between China and Spain
- INVENTORS CITY International Proceedings- 2012
Last modified: 2012-04-25 21:00:49