Digital Transformation 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 data integrity 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 accreditation preparation, technical record keeping and corrective and preventive action in their own organisation.
What delegates leave able to do
- Improve accreditation preparation within their own organisation, measured against ISO 9001
- Explain technical record keeping to someone who does not do the work
- Take ownership of corrective and preventive action rather than escalating it
- Spot where equipment calibration is failing before it becomes a finding
What the course covers
- Data integrity
- Root cause analysis
- Accreditation preparation
- Technical record keeping
- Corrective and preventive action
- Equipment calibration
- Supplier qualification
Who should attend
- quality managers
- laboratory supervisors
- quality assurance officers
- analytical chemists
