Dublin, April 15, 2026 (GLOBE NEWSWIRE) -- The "Pharmaceutical Regulatory Affairs in Africa (May 6th - May 7th, 2026)" training has been added to ResearchAndMarkets.com's offering.
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.
Who Should Attend:
This event will be of particular interest to all those who need to learn about successful marketing authorisation applications and regulatory compliance in key African areas. It will be useful as both an introductory and a refresher course on recent developments.
Key Topics Covered:
Day 1
- Basic terms and environment
- Harmonisation initiatives within Africa
- Regional presentations
- South Africa
- Namibia
- Botswana
- Zimbabwe
- Zambia
Day 2
- Malawi
- Tanzania
- Kenya
- Uganda
- Nigeria
- Ghana
- Maghreb Countries - Algeria, Morocco, Tunisia
- Final discussion session
CPD Hours: 12
Speakers
Salma Ismail
Salma Ismail is the CEO of Twinz Regulatory Affairs Pharmacist Consultants based in South Africa. Salma has over 20 years of experience within the Pharmaceutical Industry and in Regulatory Affairs, which includes understanding of legislation, technical issues, marketing regulations and training people within the pharmaceutical industry.
Makram Nehme
Makram Nehme is a Regional Regulatory Consultant having relevant experience with multiple multinationals including Parexel international, based in Lebanon. He has more than 10 years' experience in the Pharmaceutical and Medical Device Industry and is a Regulatory Expert covering the Middle East and North African markets. His experience includes negotiations with the Ministry of Health and Drug Agencies in the region, as well as training of key personnel and he has a proven record in regulatory submissions, analysis, product pricing and reimbursement across the MENA region.
For more information about this training visit https://www.researchandmarkets.com/r/xwyrjm
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