Root Cause Analysis Auditing and Assurance
3 days|Delivered on request
This programme is written from the assurance side. Delegates learn to test whether laboratory design and document control are working as claimed, and how to evidence the conclusion. Assurance work is under scrutiny because quality managers are often appointed from the bench without management training. Delegates leave able to work confidently with corrective and preventive action, equipment calibration and non-conformance management in their own organisation.
What delegates leave able to do
- Make a decision about corrective and preventive action without waiting for a specialist, measured against ISO 17025
- Bring equipment calibration into line with current good practice
- Put non-conformance management on a footing they can defend to a reviewer
- Improve data integrity within their own organisation
What the course covers
- Laboratory design
- Document control
- Corrective and preventive action
- Equipment calibration
- Non-conformance management
- Data integrity
- Sample handling and chain of custody
Who should attend
- laboratory technicians
- quality managers
- quality assurance officers
- laboratory managers
- analytical chemists
