This document offers a guide to aid procurement agencies in securing safe and effective pharmaceuticals of high quality. It emphasizes the importance of quality assurance in the procurement process, highlighting the risks of acquiring substandard or counterfeit products. The guide is structured into six modules, each addressing different aspects of procurement:
General Requirements: Outlines the foundational quality assurance systems for procurement agencies. Prequalification: Provides guidelines for evaluating product needs and assessing the offerings from manufacturers. Purchasing: Describes the principles and strategies of procuring pharmaceutical products. Receipt and Storage: Offers best practices on how to receive, store, and maintain the quality of pharmaceutical products. Distribution: Covers the best practices for distributing pharmaceutical products efficiently and safely. Reassessment: Discusses the continuous monitoring and re-evaluation of products and associated activities.
The document emphasizes the significance of a harmonized system for procuring pharmaceuticals, ensuring patient safety, financial efficiency, and the credibility of procurement agencies. It serves as a vital resource for agencies and organizations involved in the pharmaceutical procurement process.
You can submit a specific query to QUAMED experts by clicking on the button below. We will send relevant answers directly to your mailbox.
Submit Query
The information provided on this Web site is not official U.S. Government information and does not represent the views or positions of the U.S. Agency for International Development or the U.S. Government.
ISO 9001:2015 - FS766975
© 2024 - QUAMED
Content of this site is licensed under a Creative Commons License- BY Attribution