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?

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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