Evaluation and Registration of Medical Products
Implement a regional joint assessment procedure in order to improve access to quality and safe medicines in the ECOWAS region.
Electronic Common Technical Document (eCTD)
electronic common technical document (eCTD) is an interface and international specification for the pharmaceutical industry to agency transfer of ...
Good Manufacturing Practices and Inspections
Harmonize the medicines inspection and Good Manufacturing Practice system that ensure timely access to safe, efficacious, quality and affordable medicines for the people of the West African region.
Clinical Trials, Pharmacovigilance and Drug Safety
Assess safety and quality of pharmaceutical products throughout their shelf life and at all levels of the supply chain
Quality Control Laboratories
Ensure the accreditation and functioning of Quality Control Laboratories in line with National, Regional and International standards for NMRAs handling the regulation of medicines in ECOWAS member states.
Quality Management Systems
Ensure implementation of Quality Management Systems in line with national and international standards for NMRAs handling the regulation of medicines in the West African region.
Information Management Systems
Implement a harmonized Information Management System for the Medicines Registration process that supports availability and access to safe, efficacious, quality and affordable medicines for public health interventions in the West African region.
Policy, Legislation, Regulatory Frameworks
Oversee the effective implementation of a harmonized Legal and Legislative System (LLS) for medicines regulation in West African Member States.
Procurement of Medicines
Strengthen the procurement and distribution chain in ECOWAS through a regional strategy of procurement in medicines and vaccines.
Monitoring & Evaluation(M&E)
Contribute to improving governance of the health systems in the region through M&E
Financing
Strength the generally inadequate Health financing in the ECOWAS region to meet regional and national priority.
Import and Export of Products
Advocate for zero tariff on pharmaceutical raw materials within the ECOWAS Common External Tariff(CET)
African Medicines Regulatory Harmonization (AMRH)
The African Medicines Regulatory Harmonization (AMRH) initiative works with ECOWAS to increase access to good quality, safe and effective medicines through harmonizing medicines regulations, and expediting registration of essential medicines.
Medical Products Dossier Evaluation and Registration
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Electronic Common Technical Document (eCTD)
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Good Manufacturing Practices and Inspections
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Clinical Trials, Pharmacovigilance and Medicines Safety
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Quality Control Laboratories
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Quality Management Systems
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Information Management Systems
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Policy, Legislation and Regulation
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Procurement
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Monitoring & Evaluation
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Financing
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Import & Export of Products
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African Medicines Regulatory Harmonisation (AMRH)
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We work with regulatory bodies, international organizations and governments to deliver even more effective and successful projects and programmers. Their support has been vital in achieving our vision, mission, and objectives.
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