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INTRODUCTION This document has been prepared for the purchase of all types of Drugs and Vaccines. The procedures of this document shall be subjected to the approved laws in Iraq and the (Dissolved)
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Annex 6 WHO Good refers to a section of the World Health Organization's guidelines that outlines the requirements for good manufacturing practices in the production and distribution of therapeutic products.
Manufacturers and distributors of therapeutic products that fall under WHO regulations must file Annex 6 WHO Good.
To fill out Annex 6 WHO Good, entities must provide details about their production processes, quality control measures, and compliance with WHO guidelines as per the specified format.
The purpose of Annex 6 WHO Good is to ensure that therapeutic products are manufactured and distributed according to established safety, quality, and efficacy standards.
Information that must be reported includes the manufacturing processes, quality control protocols, facility details, and any relevant certifications.
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