ISO 17025 Implementation: Tools and Techniques
3 days|Delivered on request
This is a hands-on programme. Delegates spend most of the time working through corrective and preventive action and quality management systems on live scenarios rather than listening to theory about them. The practical emphasis is deliberate: method validation is frequently treated as paperwork rather than as evidence, and reading about the method has repeatedly proved insufficient. Delegates leave able to work confidently with document control, data integrity and accreditation preparation in their own organisation.
What delegates leave able to do
- Put document control on a footing they can defend to a reviewer, measured against good laboratory practice
- Improve data integrity within their own organisation
- Spot where accreditation preparation is failing before it becomes a finding
- Make a decision about method validation without waiting for a specialist
What the course covers
- Corrective and preventive action
- Quality management systems
- Document control
- Data integrity
- Accreditation preparation
- Method validation
- Equipment calibration
Who should attend
- quality managers
- internal auditors in laboratories
- laboratory managers
