— Course series

Regulatory Affairs - Africa Certification

Unlock the next frontier of pharmaceutical growth.
Master regulatory pathways across Africa's key markets and the new African Medicines Agency (AMA). Learn country-specific requirements, AVAREF joint reviews, WHO PQ pathways, and the strategies that get products approved across the continent.
This 10-module track covers the African Medicines Regulatory Harmonization (AMRH), ZAZIBONA, country-level pathways across South Africa, Nigeria, Egypt, East Africa, North Africa, West and Central Africa, and the strategic toolkit for accessing 1.4 billion patients.
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17 modules

Comprehensive, self-paced curriculum covering every core competency.

CPD-certified

Accredited programs recognized by sponsors, CROs, and health authorities.

10 Expert instructors

Direct access to working CRAs and CRCs who guide your real-world growth.

12 months access

Full year of platform access from enrollment — learn on your schedule.
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— What's included

Master regulatory pathways across Africa

Comprehensive, CPD-certified training in pharmaceutical regulatory affairs across Africa's key markets — from country-level requirements to the new African Medicines Agency (AMA).

  •  Country-by-country pathways

    Deep-dive modules on Nigeria NAFDAC, South Africa SAHPRA, Kenya PPB, Egypt EDA, Ghana FDA, and Morocco DMP — registration, variations, renewals.

  • AMA & Continental harmonization

    Master the African Medicines Agency framework, AVAREF joint scientific reviews, and the African Medicines Regulatory Harmonization (AMRH) initiative — the future of African pharma.

  • Africa Submission-Ready Skills

    Build the SAHPRA, NAFDAC, EAC-MRH, and AMA-aligned submission skills sponsors and local representatives hire for — mapped to WHO-AFRO, ICH, and national authority expectations across English- and French-speaking Africa.

Course Curriculum

Bundle offer