Posted 13 December 2017
By Sharry Arora, Bhaskar Saxena
The article discusses best practices for a manufacturer to stay 'inspection ready' on a day-to-day basis with a focus on how to prepare for and successfully manage FDA inspections from start to finish.
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Categories: Drugs, Compliance, Manufacturing, Features, US, FDA
Tags: Inspections, GxP, Quality Management System, QMS, CAPA, CMC, Validation, Form 483, Quality Assurance