Pharmaceutical Regulatory Affairs in Africa
The value of the African pharmaceutical market is increasing and growth is expected to continue at a rapid pace. There are a number of distinct markets within the region, each with their own economic and regulatory characteristics. This event will explore the key areas of African regulatory affairs, including the new SAHPRA guidelines in South Africa, and will focus on practical aspects to assist with your regulatory activities. The expert speakers will share their knowledge of working in the region and the programme will include interactive discussion sessions to enable you to share experiences with other delegates.
Covering the key regions of Algeria, Botswana, Ethiopia, Ghana, Kenya,
Malawi, Morocco, Mozambique, Namibia, Nigeria, South Africa, Tanzania,
Tunisia, Uganda, Zambia, Zimbabwe.
Benefits of attending:
- Gain an overview of the regulatory requirements within African countries
- Understand requirements for company and product registration
- Learn practical information on compiling dossiers
- Discuss the new SAHPRA guidelines in South Africa
- Explore the harmonisation and cooperation initiatives in Africa, including the new African Medicines Agency
Participants will receive a course material folder containing comprehensive documentation provided by the speakers, which will be a valuable source of reference for the future.
Upcoming start dates
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Reviews by course attendees
Average rating 4.6
Very good, especially the opportunity to ask specific questions to the speaker with so much experience on the field.
Fantastic speaker, really experienced and able to give real 'examples' of dealing with the authorities. Lovely to be able to ask questions so readily (rather than at the end of ...
Presentations/content and speakers were well rounded and provided valuable information for my job that showed the experience they had to give me confidence in the information pr...