Artificial Intelligence in Document Control
3 days|Delivered on request
This programme examines how the practice is shifting, and what delegates should adopt, adapt or ignore. It works through internal auditing and root cause analysis as they stand today and where they are heading. The shift is worth understanding because an accreditation finding can stop a laboratory trading in a way no other quality failure does. Delegates leave able to work confidently with technical record keeping, data integrity and non-conformance management in their own organisation.
What delegates leave able to do
- Explain technical record keeping to someone who does not do the work, measured against SANAS accreditation requirements
- Make a decision about data integrity without waiting for a specialist
- Put non-conformance management on a footing they can defend to a reviewer
- Review method validation and say plainly whether it is working
What the course covers
- Internal auditing
- Root cause analysis
- Technical record keeping
- Data integrity
- Non-conformance management
- Method validation
- Accreditation preparation
Who should attend
- quality managers
- technical signatories
- quality assurance officers
- laboratory technicians
