Africa niche CRO


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.
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Submit RFP for FREE consultation.


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.

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Contact Us

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

We can help with Protocol design, Regulatory affairs, Site selection, Clinical monitoring, Site management, Data management & much more.
Please fill out the Form below
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Expand your practice and build your career with
clinical research.

ACE Research is always seeking to expand our network of principal investigator partners. If you are interested in participating in clinical research, we offer the opportunity to join an accomplished investigative clinical research team.
Please fill out the Form below
 
SUBMIT
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