Preparing for and Managing FDA Inspections
By Sharry Arora, Bhaskar Saxena -
Published 13 December 2017
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.
Categories: Features, US, FDA, Compliance, Drugs, Manufacturing
Tags: Inspections, GxP, Quality Management System, QMS, CAPA, CMC, Validation, Form 483, Quality Assurance