Developing Documents and Records to meet the Requirement of ISO 17025 - 2016 is a seminar that covers topics such as:
- How do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?
- Become accredited? Where do you start?
- Maintaining the QMS and providing evidence of compliance
- Developing 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
Developing Documents and Records to meet the Requirement of ISO 17025 - 2016 brings together attendees from:
- Laboratory Quality Development
- Laboratory Management/Supervision
- Laboratory Quality Control
- Laboratory Quality Management
- Analytical Support
