Improving PAT Validation
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Improving PAT Validation
Add bookmarkQualification of equipment and validation of analytical methods are critical components for the implementation of process analytical technology (PAT). Martin Warman, Scientific Fellow, Analytical Development at Vertex Pharmaceuticals, joins Andrea Charles from Pharma IQ, to discuss the effects of apply PAT to pharmaceutical manufacturing and how to successfully validate PAT methods. Warman also shares his insights on how to select the right partner in the validation process.
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Tags:
Martin Warman
Vertex Pharmaceuticals
PAT
QbD
process analytical technology
Quality by Design
validation of PAT methods
laboratory based analytical methods
Change Control
verification of method validity
