DRAFT AGENDA OUTLINE
Session 1
What is VPHP? What are the important considerations? And overview of pertinent regulations
Session 2
Cycle development and approaches to cycle development
- Min/max, thermal/cold spot, smoke distribution
Session 3
Cycle validation and approaches to validation
- Above below and at dew point
Session 4
Chemical Indicators, Biological Indicators and Enzyme Indicators – what each one of them are, when to use them, what they tell you
Session 5
Cleaning & loading isolator
Session 6
Glove selection, integrity testing, validation, glove shelf life and, glove failure process
Session 7
Case Study: Overcoming validation problems
To register your interest please click here maxine@pharmig.org.uk
