How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 2019 is a webinar that covers topics such as:
- 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
How to Conduct a Quality Management System Audit to ISO/IEC 17025:2017 2019 is intended for:
- QA Managers
- Laboratory Managers
- Laboratories accredited to ISO/IEC 17025:2005
- QC Analysts
- Laboratories seeking to become accredited to ISO/IEC 17025
