The United States Food and Drug Administration inspects pharmaceutical companies and device manufacturers to assess if controls, procedures and practices for development and manufacturing of products are in compliance with FDA regulations.
This SOP will help companies to understand the required preparation steps, procedures to follow during and follow up after FDA inspection. The document contains various responsibilities to be involved in the inspection, the procedures to review and contains 3 checklist formats required for easy implementation.
Product ID : KTCP236
Format: Editable Word document (15 Pages)
Price : 
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