Abstract
Computerized system validation (CSV) in good practice (GxP)-regulated laboratories is alleged to take ages and generate piles of paper to keep inspectors and auditors quiet. To the rescue is the draft FDA guidance on computer software assurance (CSA). But...is this really the case?
Publisher
Multimedia Pharma Sciences, LLC
Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry
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