Navigating Africa's Regulatory Landscape with Confidence
ECP is your trusted partner for regulatory intelligence, clinical research, and cGMP support across African markets. Nairobi-based experts with 15+ years experience.
About Us
Your Partner in African Pharmaceutical Excellence
Who We Are
Headquartered in Nairobi, Kenya, ECP is a private limited company incorporated under the Companies Act 2015. We are a consortium of professionals with over 15 years of experience in assisting global pharmaceutical companies in achieving regulatory compliance, clinical research, and cGMP standards. We provide our clients with a comprehensive portfolio of services optimized to meet the standards of African Medicines Regulatory Authorities (AMRAs).
Our Mission
Our mission is to streamline the expensive and time-consuming process of bringing effective and reliable medicines to market and ensuring their continued availability for the benefit of patients.
Why Choose Us
Extensive Experience
With over 15 years of expertise, we have a proven track record of helping global pharmaceutical companies achieve regulatory compliance and clinical research excellence.
Proven Success
ECP has completed numerous projects with leading pharmaceutical companies, delivering successful outcomes in regulatory intelligence, clinical trials, and more.
Specialised Knowledge
Our multidisciplinary team specializes in end-to-end regulatory solutions with in-depth knowledge of African Medicines Regulatory Authorities (AMRAs).
Commitment to Innovation
We are dedicated to shortening the time-to-market for effective medicines through innovative and efficient processes.
Client-Centric Approach
We prioritize our clients' needs, tailoring our services to meet their specific requirements and fostering long-term partnerships.
Regional Expertise
Headquartered in Nairobi, we have a deep understanding of the regulatory landscape in Africa, providing targeted solutions for the region.
Our Services
Comprehensive regulatory and clinical solutions tailored for African markets
Strategic Regulatory Intelligence
Stay ahead of evolving regulatory environments in African markets with our strategic intelligence services.
Regulatory Affairs
Comprehensive regulatory affairs management from new product authorizations to lifecycle management.
Clinical Research
Clinical trial support, site selection, regulatory approvals, and pharmacovigilance services.
cGMP Compliance
GMP audits, quality system implementation, and preparation for regulatory inspections.
Regulatory Medical Writing
Expert delivery of clear, concise, and compliant regulatory and medical writing services.
Labeling & Artwork
End-to-end labeling services and comprehensive solutions for artwork management.
Pharmacovigilance
Ensuring drug safety and efficacy through comprehensive pharmacovigilance services.
Our Clients
Trusted by leading pharmaceutical companies and research organizations
Track Record
Successful regulatory approvals and clinical research projects across Africa
Grünenthal Pharmaceutical Project
Provided regulatory intelligence and guidance for branded generic registrations and regulatory maintenance in Kenya.
Read Case StudyWorld Bank - EBA Project
Delivered regulatory framework intelligence for the Efficient Business for Agriculture (EBA) project, impacting veterinary product registration and importation in Kenya.
Read Case StudyGSK Projects
Supported PAREXEL's GSK Vx Divestment project, regulatory strategy for Kenya and Nigeria, and restructuring of pharmaceutical operations in Sub-Saharan Africa.
Read Case StudyPAREXEL Multi-Client Projects
Provided consulting services for Novartis, Merck, P&G, Angelini, MSD and LEO Pharma including clinical trial label knowledge and regulatory strategy development.
Read Case StudyHealth Advances Boston
Conducted regulatory intelligence for vaccine development and regulatory strategy in Ethiopia, Nigeria, and the Democratic Republic of the Congo.
Read Case StudyLeadership Team
Experienced professionals with deep expertise in African regulatory landscapes
Our Regional Coverage
Eastern Africa (EAC & IGAD)
Dr. Elly Onyango Obonyo - Technical Director Regulatory Affairs
Based in Nairobi, Kenya | 15+ years experience
Western Africa (ECOWAS)
Our dedicated team provides expert regulatory support in Western Africa.
Southern Africa (SADC)
Our dedicated team provides expert regulatory support in Southern Africa.
Global Operations
Nancy Akoth - ECP Director & Independent Consultant
Based in Virginia, United States | 8+ years experience
Dr. Elly Onyango Obonyo
15 years in pharmaceutical regulatory affairs
Nancy Akoth
Over 8 years in data analysis and compliance
Our Team in Southern Africa
Years of experience in pharmaceutical regulatory affairs
Our Team in Western Africa
Extensive experience in pharmacovigilance
Client Testimonials
What our clients say about working with us
"ECP's expertise in navigating the complex regulatory landscape across Africa was instrumental in our product's successful registration in 5 countries."
Michael Johnson
Director, Global Pharma Inc.
"Working with ECP on our clinical trial was a seamless experience. Their local knowledge saved us significant time and resources."
Sarah Roberts
Clinical Operations Manager
Get in Touch
globalaffairs.elymedicarepharma@gmail.com
+15743440684