Africa CRO Clinical Trial Services
Be 100% assured that everything at your trial site is being done the right way — and that your critical deliverables will be ready on-time and at the highest quality.
Cost effective
Implement the site activities correctly, the first time to avoid course corrections and burn on budget.Accelerate
Mitigate risks and eliminate unwanted impact on the project timeline, performance, and budget.Confidence
Get quality and validated data that boost confidence and rapid market access.Peace of mind
Get help with Regulatory audits and inspection readiness for total peace of mind.Services
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.
