Phase lV / Post-Approval

As regulatory requirements grow, Phase lV trials are becoming critical and costly stepping-stones to market release for drugs and medical devices. ACE Research's team is a proven solution to managing thousands of subjects in post-marketing studies to determine additional safety information, or pharmacovigilance, regarding the risks, benefits, and optimal usage of drugs and medical devices.

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
SUBMIT
close-link

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
close-link