Support Mission for Pharmaceutical Industries to Comply with EU Good Manufacturing Practices (GMPs)
A support mission for pharmaceutical industries to comply with European Union Good Manufacturing Practices (EU GMPs) has been launched to offer Tunisian private pharmaceutical industries, manufacturing human-use medicines and already exporting to the MENA region or African markets, the opportunity to conform to European quality requirements, a crucial condition for integrating European supply chains.
Benefits of the Mission
This initiative provides access to international expertise for a documentary and on-site diagnosis according to the European EUDRALEX.V4 reference framework. Additionally, it offers international expertise to develop an action plan to address non-conformities observed in the diagnostic report.
Program Context
This program is part of the "Support for the Modernization of Tunisian Industry" project, under the "Qualitative Growth for Employment" initiative. It is funded by the German Federal Ministry for Economic Cooperation and Development and the EU in Tunisia, and implemented by GIZ Tunisia in partnership with the Ministry of Industry, Mines, and Energy.
Interested in Participating?
If this mission interests you, apply now via this link.