How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 2019

Topics

• What are the new requirements of ISO/IEC 17015:2017?
• Have the rules changed? Recall the differences between ISO/IEC 172025:2005 and the newly revised version, ISO/IEC 17025:2017
• 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?
• Identify the new documents and records required by the standard
• Defining a QMS
• Implement a quality documentation transition plan to ensure compliance with the newly revised standard
• New and revised Quality Management Requirements
• Management Components of a QMS
• New and revised Technical Requirements
• Technical Components of a QMS
• Ensuring analytical competency
• Method Selection, Validation and Verification
• Identifying adjustments to your existing ISO/IEC 17025:2005 Quality Documentation

Who should Attend

• QA Managers
• Laboratory Managers
• Laboratories accredited to ISO/IEC 17025:2005
• QC Analysts
• Laboratories seeking to become accredited to ISO/IEC 17025