Every case study below represents a delivered BethAri engagement, backed by formal project reports, signed contracts, or verified client outcomes. We combine deep regional expertise across West Africa with executive industry consulting across the UK and Europe.
National Medicines Regulators Assessed
ECOWAS Member States Mapped
Regulators Now ISO 9001 Certified
Annual Savings Realised
On-site QMS assessments of 17 national medicines regulatory authorities, custom roadmaps to ISO 9001:2015, and regional validation workshops and training across ECOWAS member states. Five assessed authorities subsequently achieved full ISO 9001:2015 certification.
A region-wide study mapping, quantifying, and evaluating local pharmaceutical manufacturing capacity and policy constraints across all 15 ECOWAS member states, with strategic recommendations validated by regional stakeholders.
WAHO and the World Bank required an independent, rigorous end-of-project appraisal of the US$3m West African Medicines Regulatory Harmonisation (WA-MRH) initiative to evaluate achievements, governance, and long-term sustainability across 15 countries.
Process mapping and an AI/automation implementation roadmap for global manufacturing change submissions, enabling the client to realise over €2m in recurring annual efficiency savings.
A UK-based clinical research organization required independent verification of a key investigational medicines distribution vendor to ensure strict compliance with Good Distribution Practice (GDP) and Good Clinical Practice (GCP).
A global consumer healthcare company experienced persistent quality compliance gaps across international manufacturing sites, with site quality culture and audit readiness scoring below 50%.
In addition to our major case studies, BethAri’s leadership has delivered foundational capacity-building engagements across West Africa:
Facilitated joint Good Manufacturing Practice training and technical alignment workshops for NAFDAC inspectors and Nigerian pharmaceutical manufacturers.
Contributed expert technical authorship to the ECOWAS Regional Pharmaceutical Plan published by WAHO.
Delivered specialized capacity training for senior NAFDAC assessors on evaluating Module 3 (Quality/CMC) of Common Technical Document registration dossiers.
Conducted advanced GMP compliance training for pharmaceutical industry executives and regulatory inspectors.
