Artificial Intelligence in Technical Record Keeping
3 days|Delivered on request
This programme examines how the practice is shifting, and what delegates should adopt, adapt or ignore. It works through supplier qualification and document control as they stand today and where they are heading. The shift is worth understanding because method validation is frequently treated as paperwork rather than as evidence. Delegates leave able to work confidently with laboratory design, corrective and preventive action and accreditation preparation in their own organisation.
What delegates leave able to do
- Put laboratory design on a footing they can defend to a reviewer, measured against ISO 9001
- Improve corrective and preventive action within their own organisation
- Make a decision about accreditation preparation without waiting for a specialist
- Take ownership of quality management systems rather than escalating it
What the course covers
- Supplier qualification
- Document control
- Laboratory design
- Corrective and preventive action
- Accreditation preparation
- Quality management systems
- Laboratory safety
Who should attend
- laboratory supervisors
- quality assurance officers
- laboratory technicians
- quality managers
