This training program will discuss in details the new requirements of ISO/IEC 17015:2017 laboratory accreditation standard and their impact on quality management system. It will provide you with an overview of the salient differences and similarities between the old and the new standard and provide advice on what you must do to meet the requirements each of the elements.
Why Should You Attend:
Many laboratories have successfully developed and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Some are still struggling to get accredited and even those already accredited still have issues as evidenced by the number of non-conformances cited during the subsequent biannual audits. Have the rules changed? What are the new requirements of ISO/IEC 17015:2017? How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?Areas Covered in the Webinar:
- What is ISO/IEC 17025
- How is ISO/IEC 17025:2017 different from ISO/IEC 17025:2005
- What are the most significant changes between 2005 and 2017 versions?
- What must my lab do to comply
- Preparing for an Audit
Who Will Benefit:
- Laboratory Managers
- QA Managers
- QC Analysts
- Analytical Support Personnel
- Laboratory Quality Management Staff
Course Provider
Michael Brodsky,
