Leading Data Integrity Teams
3 days|Delivered on request
This programme is for the person accountable for the work rather than the person doing it. It covers supplier qualification and internal auditing from the position of someone who must review, approve and answer for the output. Managers carry this because method validation is frequently treated as paperwork rather than as evidence, and the accountability does not delegate cleanly. Delegates leave able to work confidently with non-conformance management, document control and laboratory safety in their own organisation.
What delegates leave able to do
- Explain non-conformance management to someone who does not do the work, measured against SANAS accreditation requirements
- Take ownership of document control rather than escalating it
- Bring laboratory safety into line with current good practice
- Put quality management systems on a footing they can defend to a reviewer
What the course covers
- Supplier qualification
- Internal auditing
- Non-conformance management
- Document control
- Laboratory safety
- Quality management systems
- Equipment calibration
Who should attend
- quality assurance officers
- quality managers
- internal auditors in laboratories
- analytical chemists
- laboratory supervisors
