Objectives

Patient Safety
Promoting patient safety by strengthening regulatory practices and ensuring reliable oversight in healthcare systems.

Trial Transparency
Enhancing the timeliness and transparency of clinical trials conducted across Africa for better outcomes.

Innovation & Research
Stimulating innovation and advancing scientific research across Africa to support health and development.


Review & Inspection Quality
Improving efficiency and quality of regulatory reviews and inspections to build trust and accountability.

Regulatory Harmonization
Accelerating the African Medicines Regulatory Harmonization (AMRH) process to align all Regional Economic Communities.(RECs)

Emergency Preparedness
Strengthening preparedness across the continent, in RECs, and in individual countries to respond to emergencies.
Governance Structure
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- AMRH Steering CommitteeStrategic Director & Oversight
AMRH Steering Committee
Strategic Director and Oversight
Strategic direction & oversight. Responsible for setting AVAREF’s strategic direction, workplans, and priorities. It includes representatives from all 8 African Union Regional Economic Communities (RECs) to ensure continental inclusivity and alignment.
- AVAREF AssemblyHighest decision-making body
AVAREF Assembly
Highest decision-making body
The highest decision-making body, composed of all Heads of National Regulatory Authorities (NRAs) and National Ethics Committees (NECs). It provides continental-level leadership and endorses strategic directions.
- Technical Coordinating CommitteeCoordination and Oversight
Technical Coordinating Committee
Coordination and Oversight
Coordination & Acts as the main scientific and technical advisory body. It ensures coherence across AVAREF’s workstreams, guides technical initiatives, and reviews deliverables from the working groups.
- Antimicrobial Resistance (AMR)
Antimicrobial Resistance (AMR)
Focuses on regulatory preparedness for clinical trials addressing AMR, including antibiotics, diagnostics, and stewardship interventions. It contributes to WHO’s One Health approach and AMR strategic objectives.
- Vaccine R&D
Vaccine R&D
Supports regulatory readiness for early-stage vaccine development and clinical trial design. The group collaborates with product developers, research centres, and WHO partners to ensure ethical and scientifically rigorous vaccine R&D in Africa. It plays a critical role in pandemic preparedness, equitable innovation, and the adoption of novel platforms and technologies.
- Controlled Human Infection Models (CHIM)
Controlled Human Infection Models (CHIM)
Develops frameworks for the ethical and regulatory oversight of CHIM studies across African countries, ensuring safety and compliance with international standards.
- Snakebite Treatment (SBT)
Snakebite Treatment (SBT)
Works on protocols and regulatory guidance for clinical trials evaluating antivenoms and other snakebite interventions, contributing to WHO’s NTD roadmap.
- AVAREF SecretariatCoordination and Support
AVAREF Secretariat
Coordination and Support
Located at the WHO Regional Office for Africa, the Secretariat is responsible for day-to-day coordination, partner engagement, documentation, knowledge-sharing, capacity-building activities, and resource mobilization.
The AVAREF Secretariat and Key Functions
Housed within the WHO Regional Office for Africa in Brazzaville, the Secretariat coordinates AVAREF’s operations, partnerships, and strategic implementation.
Clinical Trial Reviews
Organizing joint and assisted clinical trial reviews, both virtually and in person
Training & Education
Coordinating training workshops, continuing education, and specialized webinars
Communication & Engagement
Managing communication, outreach, and partner engagement
Guidelines & Tools
Drafting and publishing guidelines, emergency frameworks, and technical tools
AMA & System Strengthening
Supporting the African Medicines Agency (AMA) and strengthening national systems
Expert Roster & Specialists
Maintaining the Roster of Experts, mobilizing technical specialists across clinical trial domains