Clinical Trial Applications
Expert assistance with submissions to ethics committees and regulatory authorities. We ensure your applications are complete, compelling, and compliant with local requirements.
Clinical Research Services
Advancing healthcare through expertly managed clinical trials across Africa. From trial design to regulatory submissions, we ensure your research is conducted efficiently, ethically, and in full compliance.
Service 03 / 0703What we deliver
Comprehensive Clinical Research Support
End-to-end management of your clinical trials with local expertise
Site Selection & Management
Identify and manage the best clinical trial sites for your study. Our extensive network ensures access to qualified investigators and diverse patient populations.
Pharmacovigilance & Safety
Robust safety monitoring throughout your trial. We ensure patient safety and data integrity with comprehensive pharmacovigilance services.
Patient Recruitment
Leverage our local networks to recruit diverse patient populations efficiently. We understand cultural nuances and community engagement strategies.
Data Management
Ensure data quality and integrity with our rigorous data management protocols. We maintain the highest standards for clinical data collection and analysis.
Regulatory Compliance
Navigate complex regulatory requirements across multiple African jurisdictions. We ensure your trial meets all local and international standards.
Why ECP
Local expertise. Global standards.
A consortium of professionals with over 15 years of experience and in-depth knowledge of African Medicines Regulatory Authorities and the standards they apply.
- Nairobi-based specialists with regional reach across 25+ countries
- A multidisciplinary team covering regulatory, clinical, safety and quality
- A track record with leading pharmaceutical organisations
How we work
Our Clinical Research Process
A proven methodology for successful clinical trials
1
Protocol Development
Design robust trial protocols tailored to African contexts
2
Regulatory Submissions
Prepare and submit applications to ethics committees and authorities
3
Site Activation
Select, qualify, and activate clinical trial sites
4
Trial Execution
Manage day-to-day operations and monitor progress
5
Data Analysis
Collect, validate, and analyze clinical data
Continue exploring
Other ECP services.
04
cGMP Compliance
GMP audits, quality system implementation and preparation for regulatory inspections.
05Regulatory Medical Writing
Clear, concise and compliant regulatory and medical writing, delivered by expert writers.
06Labeling & Artwork
End-to-end labeling services and comprehensive solutions for artwork management.
Begin
Ready to Start Your Clinical Trial?
Partner with ECP for expert clinical research management across Africa. Tell us about your product and target markets and we will respond with a clear next step.