Fees: £70 PHARMIG MEMBERS Join Now, £100 (Non Member)
Wednesday 1st June, 2pm – 3pm (GMT)
Led by Dr Tim Sandle
It is well established that regulators do not like the root causes of deviations to conclude ‘human error’ and for the resultant corrective or preventative action (CAPA) to recommend additional training. Instead, regulators expect organizations to go deeper and to unpick the underlying reasons as to why a person made an error and, from this, error risk reduction actions can be initiated.
This webinar looks at:
- The ‘what’ and ‘why’ of human error
- The ‘true’ causes of error
- Chunking and subchunking tasks
- Developing human error checklists
- Root cause analysis
- Trending error