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Registration of MedicinesZAMBIA MEDICINES REGULATORY AUTHORITYAPPLICATION FOR MARKETING Authorization
OF A MEDICINE FOR HUMAN GUIDANCE FOR THE PREPARATION AND SUBMISSION OF DOSSIERS
IN COMMON TECHNICAL
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What is zambia medicines regulatory authority?
The Zambia Medicines Regulatory Authority (ZAMRA) is a government agency responsible for regulating and controlling the manufacturing, importation, exportation, distribution, sale and use of medicines in Zambia.
Who is required to file zambia medicines regulatory authority?
All pharmaceutical companies, drug manufacturers, importers, distributors, and sellers in Zambia are required to file with the Zambia Medicines Regulatory Authority.
How to fill out zambia medicines regulatory authority?
To fill out the Zambia Medicines Regulatory Authority forms, companies must provide detailed information about the medicines they manufacture, import, distribute, and sell in Zambia.
What is the purpose of zambia medicines regulatory authority?
The purpose of the Zambia Medicines Regulatory Authority is to ensure the safety, efficacy, and quality of medicines available in Zambia, as well as to protect public health.
What information must be reported on zambia medicines regulatory authority?
Companies must report information such as the name, composition, manufacturing process, storage conditions, intended use, and side effects of the medicines they are dealing with.
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