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General Documents

GHANA

Administrative status of the product

Fast track processing of applications – 2015

Food and Drugs Board (Checklist labels A)

Food and Drugs Board (Checklist labels B)

General product specifications

Ghana labelling checklist

List of attached documents and materials

Particulars of manufacturing procedure, related controls and documentation

Sample receipt

Timelines for medicinal product re-registration

Timelines for medicinal product registration

Toxicological, Pharmacological and Clinical information

Last updated:Friday, June 17, 2016
Information presented here is subject to change. Should you have additional inputs / insights to contribute please contact info@ipasa.co.za.
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The Regulatory Resources for Africa website has been made possible by a non-prescriptive grant by Innovative Pharmaceutical Association South Africa (IPASA). . The intention of the sponsors is to create a platform where up to date and useful information concerning the medicines regulatory environment in Africa, can be shared by all

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