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.

Comprehensive Clinical Research Support

End-to-end management of your clinical trials with local expertise

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.

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.

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

Ready to Start Your Clinical Trial?

Partner with ECP for expert clinical research management across Africa

Get Started Today