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Hi Everyone!
I'm in desperate need of any kind of template (or pointing in the right
direction) that can be used in a Validation Support Package for the
installation of instrumentation into a pharmaceutical manufacturing site.
This would include Installation Qualification (IQ), Operation Qualification
(OQ) and Performance Qualification (PQ). I've checked the internet and
mostly what I get is an explanation of what it is - but not "how" to do it.
Several companies contract to do it, but we are going to do it in-house.
This would be for a process analyzer, but probably any instrumentation
would be a good starting place. I have a basic idea of what has to be done,
I just need the organization thing.
TIA!
Liz
Liz Goodwin
Technical Writer, Process Instruments
AMETEK, P&AI
liz -dot- goodwin -at- ametek -dot- com
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