Digital Transformation in Laboratory Information Management
3 days|Delivered on request
This programme examines how the practice is shifting, and what delegates should adopt, adapt or ignore. It works through accreditation preparation and laboratory safety 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 supplier qualification, quality management systems and non-conformance management in their own organisation.
What delegates leave able to do
- Review supplier qualification and say plainly whether it is working, measured against good laboratory practice
- Spot where quality management systems is failing before it becomes a finding
- Take ownership of non-conformance management rather than escalating it
- Improve document control within their own organisation
What the course covers
- Accreditation preparation
- Laboratory safety
- Supplier qualification
- Quality management systems
- Non-conformance management
- Document control
- Measurement uncertainty
Who should attend
- quality assurance officers
- laboratory managers
- quality managers
- laboratory supervisors
