Operational Expertise

We are driven by desire to help to conduct your clinical trial in a more effective way that aligns with ethical principles and business practice

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Site Assessments, Training and Recruitment

We deliver data-driven report on protocol, country and regulatory feasibility. We search our internal & external databases for targeted, high-performing, high-enrolling sites.

Regulatory Affairs

We reduce the startup timeline by providing clear instructions and expectations on how to correctly complete documents and ensure a timely submission.

Clinical Monitoring

We drive efficiency in clinical supplies and biological material transfers in all regions of Africa

We help Sponsors to Speed up Start-Up processes and Improve Efficiency of Clinical Trials in Africa

We adhere to Quality Management Plans to provide high quality data. Our monitors ensure compliance with clinical trial protocol during the entire clinical development cycle, which in turn leads to cost efficiency.

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Need help setting your next clinical trials for success in Africa?

Contact us for Protocol design, Regulatory Strategy, High enrolling sites & Investigators, Clinical Monitoring, Site management, Data management, Biologic material transfer  & much more.
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