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December 17, 2019

Accelerating Study Start-up Regulatory Submission in Sub-Saharan Africa

Conducting clinical trials in Africa has many benefits. But sometimes the regulatory approval can be a drag.

Learn how ACE Research uses proprietary regulatory intelligence database, country-specific guidelines, and project-specific regulatory tracker to streamline

  • the collection of site essential documents,
  •  QA regulatory package
  • submission of the final dossier to the ethics committees and national regulators,

We ACE regulatory submissions to the ethic committee and the regulatory authorities, making the process

  • faster,
  • predictable
  • aligned to the format and style of Africa regulators



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

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